search
Back to results

Evaluation of Retina in Patients With Glaucoma Using Topical Prostaglandins Undergoing Trabeculectomy Surgery (TRAB)

Primary Purpose

Glaucoma

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Trabeculectomy surgery
Sponsored by
Universidade Federal de Goias
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Glaucoma focused on measuring prostaglandin analogue, macular edema, trabeculectomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Clinical Diagnose's of Primary Glaucoma Primary Open Angle Glaucoma Primary Closed Angle Glaucoma Normal Pressure Glaucoma Pigmentary Glaucoma Pseudosfoliative Glaucoma) Changes in the visual field Typical defect compatible with glaucomatous lesion and/or typical anatomical impairment of the optic disc or retinal nerve fiber layer Hoyt's sign Optic disc cupping ratio greater than 0.7 Defect located in the neural rim or cupping asymmetry Indication for TRAB with MMC at the physician's discretion (target IOP not established with maximum tolerable clinical medication or impossibility of using medication due to allergies and/or financial conditions) The operated eyes needed a reduction in IOP by at least 20% in relation to the baseline IOP in the last postoperative period (PO30) Absence of the use of any ocular hypotensive medication. Exclusion Criteria: Any pathology that could interfere with the test results cataract (crystalline opacity) corneal edema (such as leucoma, ulcers, keratopathies) poor quality of exams (≤ 5/10) any past macular pathology (such as macular hole, diabetic maculopathy, age related macular disease); Use of diamox Advanced glaucoma with maximal therapy Advanced glaucoma with impaired fixation Any surgical complications including hypotonia (IOP < 6 mmHg) at any assessment Performing combined cataract and glaucoma surgery History of cataract surgery less than 6 months ago Need for surgical reintervention during follow-up for any reason Need for reintroduction of topical antiglaucoma therapy.

Sites / Locations

  • Centro de Referencia em Oftalmologia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Study group

Control group

Arm Description

The Study group refers to patients who are using topical prostaglandins analogues

The Control group refers to patients who discontinued the use of topical prostaglandins analogues

Outcomes

Primary Outcome Measures

Previous use of prostaglandins does not change macular thickness after trabeculectomy
The absolute variation of each variable of the macular parameters OCT in relation to the pre-op was performed and its comparison between the groups at different moments. There was equivalence in most of the evaluated comparisons. Considering the variation between pre-op and PO30, only the upper parafoveal thickness was statistically different between groups (p= 0.01). Taking into account the difference in percentage analyzing pre-op vs. PO30, only the superior parafoveal thickness showed statistical significance between groups (p=0.01).

Secondary Outcome Measures

The presence of the lens did not influence the correlations
Correlations were performed between the deltas of the thicknesses of the macular parameters between the preoperative period and the PO30 within the groups with the possible confounding factors (MD and IOP) and also controlling the intensity of the lens effect (partial correlation). There was no significant correlation in the other tests performed, as well as in relation to the possible influence of the crystalline lens in each of them.

Full Information

First Posted
August 12, 2023
Last Updated
August 17, 2023
Sponsor
Universidade Federal de Goias
search

1. Study Identification

Unique Protocol Identification Number
NCT06000280
Brief Title
Evaluation of Retina in Patients With Glaucoma Using Topical Prostaglandins Undergoing Trabeculectomy Surgery
Acronym
TRAB
Official Title
Evaluation of Macular Thickness in Patients With Glaucoma in Use of Topical Prostaglandin Analogue Undergoing Trabeculectomy With Mitomycin C
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
January 4, 2021 (Actual)
Primary Completion Date
February 28, 2023 (Actual)
Study Completion Date
March 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal de Goias

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study was to verify whether prostaglandin analogue (PA) eye drops influence the retinal thickness of glaucomatous patients undergoing trabeculectomy (TRAB) surgery. We selected eyes of patients with glaucoma with surgical indication for TRAB who were using PA eye drops and without previous retinal alterations, from the Centro de Referência em Oftalmologia (CEROF) from the Federal University of Goiás and Fundação Banco de Olhos de Goiás (FUBOG). Patients were divided into 2 groups: the study group (SG) and the control group (CG). In the CG, the PA was suspended between 30 and 60 days before the preoperative exams were performed (maximum of 15 days before surgery for both groups). All patients included were submitted to various eye exams before the procedure, and postoperatively on 3 occasions: 1 to 3 days ("PO1"), 6 to 9 days ("PO7") and 27 to 30 days ("PO30") after surgery.
Detailed Description
Purpose: The aim of this study was to verify whether topical prostaglandin analogue (PA) influence the macular thickness of glaucomatous patients undergoing trabeculectomy (TRAB) with Mitomycin C (MMC) . Design:This is a randomized, prospective, comparative clinical trial with a single surgeon and masked to the study group. Methods: We prospectively selected 40 eyes of patients with glaucoma with surgical indication for TRAB with MMC (0.4 mg/ml for 2 min) who were using prostaglandin analogue (PA) eye drops and without previous macular alterations, from the Centro de Referência em Oftalmologia (CEROF) from the Federal University of Goiás and Fundação Banco de Olhos de Goiás (FUBOG). The research had as inclusion criteria: patients with at least 18 years of age with Primary Glaucoma (Primary Open Angle Glaucoma, Primary Closed Angle Glaucoma, Normal Pressure Glaucoma, Pigmentary Glaucoma, Pseudoesfoliative Glaucoma), with changes in the visual field, typical defect compatible with glaucomatous lesion and/or typical anatomical impairment of the optic disc or retinal nerve fiber layer (such as Hoyt's sign, optic disc cupping ratio greater than 0.7, localized defect in the neural rima, or cupping asymmetry), who had an indication for TRAB with MMC at the physician's discretion (target IOP not established with maximum tolerable clinical medication and/or impossibility of using medication due to allergies and/or financial conditions). To be included, the operated eyes needed a reduction in IOP of at least 20% in relation to the baseline IOP in the last postoperative period (PO 30), and absence of the use of any ocular hypotensive medication. Exclusion criteria were any pathology that could interfere with the test results, such as: cataracts, corneal edema (such as leucoma, ulcers, keratopathies); poor quality of the OCT scan (signal strength ≤ 5/10); any past macular pathology (such as macular hole, diabetic maculopathy, age-related macular disease); use of diamox; advanced glaucoma with maximal therapy; advanced glaucoma with impaired fixation; any surgical complications including hypotonia (IOP < 6 mmHg) at any assessment; performing combined cataract and glaucoma surgery; history of cataract surgery less than 6 months ago; need for surgical reintervention during follow-up for any reason; and need for reintroduction of topical antiglaucoma therapy during follow-up. Eligible volunteers were previously randomized through the website www.randomization.com into 2 groups: study group (SG) and control group (CG). The initial objective was to include 40 eyes, 20 per group. In the SG, patients were instructed to keep using eyedrops (including PA) until the day of surgery. In the CG, patients were instructed to suspend the PA between 30-60 days after the preoperative exams were performed, which were performed a maximum of 15 days before surgery for both groups. In the CG, patients were instructed to use 01 drop of carmellose sodium 5mg/ml at the same time they used the AP before its suspension. Pseudophakic patients for more than six months were included in each group in the order of previous randomization. In the CG, patients were informed to keep the eye drops in use, and to add the other classes of ocular hypotensive drugs, if they were not using them (except miotics and oral acetazolamide), with the aim of at least remedying the loss of the ocular hypotensive effect of the PA. The individuals were evaluated, including best corrected visual acuity by the Snellen chart, slit lamp biomicroscopy (XCELL 255, Reichert Inc., Depew, NY, USA), intraocular pressure (IOP) measured in a calibrated Goldmann tonometer (CT210, Reichert Inc. , Depew, NY, USA), gonioscopy with a 4-mirror Goldman lens (Volk Optical Inc, Mentor, OH, USA), fundoscopy under mydriasis with a 78D lens (Volk Optical Inc, Mentor, OH, USA), indirect binocular ophthalmoscopy with 2.0D lens (Volk Optical Inc, Mentor, OH, USA) and Optical Coherence Tomography (OCT) with Cirrus 4000 (Zeiss Inc.), macular protocol (macular thickness and ganglion cell analysis) preoperatively ( maximum of 15 days before surgery), and postoperatively on 3 occasions: 1 to 3 days ("PO1"), 6 to 9 days ("PO7") and 27 to 30 days ("PO30"). All tests were performed by the same technician, who was trained and experienced to carry them out. All patients underwent visual field examinations (Humphrey Field, model HFA II ÿ750, Carl Zeiss-Meditec, Dublin, California, USA) prior to surgery with the Swedish Interactive Threshold Algorithm (SITA) Standard 24-2 strategy, at most up to 2 months before the procedure. Macular thickness was evaluated by spectral domain Optical Coherence Tomography (OCT) obtained using the Cirrus 4000 apparatus (Zeiss Inc.), macular scanning protocol (macular thickness and ganglion cell analysis). Calculations were made based on data from the Ganglion cell analytical program and Macular Thickness: Macular cube (6 x 6 mm - 512 A-scans x 128 B-scans centered on the fovea). The macular thickness map using the 1mm, 3mm, and 6mm circles from the Early Treatment Diabetic Retinopathy Study (ETDRS) was used to assess the thickness of the 9 subfields. The regions were designated as: parafoveal (subfields of the 3 mm rings) and perifoveal (subfields of the 6 mm rings) superior, inferior, temporal and nasal in addition to the central subfield. OCT images were excluded if the signal strength was ≤5/10, and a new scan was immediately performed. Trabeculectomy using mitomycin C consisted of opening the conjunctival base of the fornix and applying mitomycin C 0.4 mg/ml for 2 minutes, as previously described. The postoperative regimen in both groups included the use of 1% Prednisolone eye drops (Ster® União Química Farmacêutica Nacional S/A., Pouso Alegre, MG, Brazil) starting every 2 hours, with a weekly reduction for 6 weeks ( 4/4 h, followed by 6/6 h, then every 8 h, 12/12 h and once a day), Moxifloxacin eye drops (Vigamox®, AlconLabs, Fort Worth, TX, USA) every 6 h for 10 days. Statistical analysis was performed using the Statistical Package for Social Sciences program (IBM Corporation, Armonk, USA) version 26.0. The characterization of the sample was performed using absolute frequency, relative frequency, mean, standard deviation, median, minimum and maximum. Student's t test and Pearson's chi-square test were applied to the distribution of profile and macular parameters in groups with and without prostaglandin. Data normality was verified using the Shapiro-Wilk test. The delta and percentage variation were calculated at PO1, PO7 and PO30 in relation to the preoperative period. Correlation analysis was performed between thickness deltas with visual field Mean Deviation (MD) and IOP in groups with and without prostaglandin, weighted the effect of lens classification (partial correlation). The significance level adopted was 5% (p < 0.05). Initially, 40 eyes were randomly assigned to the study, of which 17 were excluded because they did not meet the eligibility criteria for the study postoperatively. Among these, 4 patients did not undergo OCT at PO1, 4 patients did not undergo OCT at PO7, 2 patients did not undergo OCT at PO30, 1 patient had a signal ≤ 5/10 of OCT at all visits, even with several repetitions of the examinations, 3 patients underwent surgical reintervention during follow-up (suture dehiscence), 2 patients had hypotonia, finally 1 patient did not present IOP reduction by at least 20% of baseline. Thus, as there was a significant reduction in the number of patients initially estimated for the sample, a new randomization was performed, using the same initial randomization process described above to achieve this objective. In the end, the evaluated sample consisted of 40 eyes from 37 patients, 20 eyes per group (20 eyes from 18 patients in the CG and 20 eyes from 19 patients in the SG).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glaucoma
Keywords
prostaglandin analogue, macular edema, trabeculectomy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a randomized, prospective and comparative clinical trial. Both the surgeon (the only one) and the technician responsible for the exams were blinded to the study groups. The patients (one or both eyes) included were from the glaucoma outpatient clinic of the Fundação Banco de Olhos de Goiás (FUBOG) or the Reference Center in Ophthalmology (CEROF) of the Federal University of Goiás (UFG) between the years 202 and 2022. All patients with glaucoma with indication for Trab with MMC and in clinical use of any PA eye drops (latanoprost, travoprost, bimatoprost or tafluprost) in the eye to be operated on for at least 6 months were considered for inclusion. The study adhered to the principles of the Declaration of Helsinki and was authorized by the Research Ethics Committee of the UFG, under the Certificate of Presentation for Ethical Appreciation NUMBER 40055620.8.1001.5083. All those included voluntarily agreed to participate by signing the Free and Informed Consent Form.
Masking
InvestigatorOutcomes Assessor
Masking Description
The techinician who performed the exams (Optical Coherence Tomography and Visual Field)
Allocation
Randomized
Enrollment
37 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study group
Arm Type
Active Comparator
Arm Description
The Study group refers to patients who are using topical prostaglandins analogues
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
The Control group refers to patients who discontinued the use of topical prostaglandins analogues
Intervention Type
Procedure
Intervention Name(s)
Trabeculectomy surgery
Intervention Description
The Trabeculectomy aims to create a permanent drainage outflow channel for the aqueous humor, connecting the anterior chamber to the sub-Tenon's space, using mitomycin C consisted of opening the conjunctival base of the fornix and applying mitomycin C 0.4 mg/ml for 2 minutes. The trabeculectomy techniques require controlled outflow of aqueous humor through a sclerostomy and a partial-thickness scleral flap to form a subconjunctival bleb. The protected strength of the flap, with or without sutures, and the strength of the episcleral tissue determine the final IOP.
Primary Outcome Measure Information:
Title
Previous use of prostaglandins does not change macular thickness after trabeculectomy
Description
The absolute variation of each variable of the macular parameters OCT in relation to the pre-op was performed and its comparison between the groups at different moments. There was equivalence in most of the evaluated comparisons. Considering the variation between pre-op and PO30, only the upper parafoveal thickness was statistically different between groups (p= 0.01). Taking into account the difference in percentage analyzing pre-op vs. PO30, only the superior parafoveal thickness showed statistical significance between groups (p=0.01).
Time Frame
Measurements were performed at preop (up to 15 days before the intervention), 1 to 3 days ("PO1"), 6 to 9 days ("PO7") and 27 to 30 days ("PO30") after surgery.
Secondary Outcome Measure Information:
Title
The presence of the lens did not influence the correlations
Description
Correlations were performed between the deltas of the thicknesses of the macular parameters between the preoperative period and the PO30 within the groups with the possible confounding factors (MD and IOP) and also controlling the intensity of the lens effect (partial correlation). There was no significant correlation in the other tests performed, as well as in relation to the possible influence of the crystalline lens in each of them.
Time Frame
Measurements were performed at preop (up to 15 days before the intervention) and 27 to 30 days ("PO30") after surgery.

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
Individuals self-identified as male and female were eligible for the study.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical Diagnose's of Primary Glaucoma Primary Open Angle Glaucoma Primary Closed Angle Glaucoma Normal Pressure Glaucoma Pigmentary Glaucoma Pseudosfoliative Glaucoma) Changes in the visual field Typical defect compatible with glaucomatous lesion and/or typical anatomical impairment of the optic disc or retinal nerve fiber layer Hoyt's sign Optic disc cupping ratio greater than 0.7 Defect located in the neural rim or cupping asymmetry Indication for TRAB with MMC at the physician's discretion (target IOP not established with maximum tolerable clinical medication or impossibility of using medication due to allergies and/or financial conditions) The operated eyes needed a reduction in IOP by at least 20% in relation to the baseline IOP in the last postoperative period (PO30) Absence of the use of any ocular hypotensive medication. Exclusion Criteria: Any pathology that could interfere with the test results cataract (crystalline opacity) corneal edema (such as leucoma, ulcers, keratopathies) poor quality of exams (≤ 5/10) any past macular pathology (such as macular hole, diabetic maculopathy, age related macular disease); Use of diamox Advanced glaucoma with maximal therapy Advanced glaucoma with impaired fixation Any surgical complications including hypotonia (IOP < 6 mmHg) at any assessment Performing combined cataract and glaucoma surgery History of cataract surgery less than 6 months ago Need for surgical reintervention during follow-up for any reason Need for reintroduction of topical antiglaucoma therapy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leopoldo Magacho dos Santos Silva, Doctor
Organizational Affiliation
Universidade Federal de Goias
Official's Role
Study Director
Facility Information:
Facility Name
Centro de Referencia em Oftalmologia
City
Goiânia
State/Province
Goias
ZIP/Postal Code
74605-020
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The data collected in the exams performed in the study and the data of the results will be made available
IPD Sharing Time Frame
Data can be shared 6 months after publication
IPD Sharing Access Criteria
Data sharing can be done after the consent of the main investigator of the study signed and sent by e-mail. Study principal investigator will review sharing requests
IPD Sharing URL
https://www.gov.br/governodigital/pt-br/governanca-de-dados/regras-de-compartilhamento_v1-0.pdf
Citations:
PubMed Identifier
8532944
Citation
Motero Carrasco J. [A comparative study of the efficacy of lisinopril versus quinapril in controlling light to moderate arterial hypertension. A follow-up with ABPM]. Rev Esp Cardiol. 1995 Nov;48(11):746-53. Spanish.
Results Reference
background
PubMed Identifier
22134362
Citation
Yonekawa Y, Kim IK. Pseudophakic cystoid macular edema. Curr Opin Ophthalmol. 2012 Jan;23(1):26-32. doi: 10.1097/ICU.0b013e32834cd5f8.
Results Reference
background
PubMed Identifier
34285468
Citation
Vessani R, Frota T, Shigetomi G, Correa P, Mariottoni EB, Tavares I. Structural Changes in the Optic Disc and Macula Detected by Swept-Source Optical Coherence Tomography After Surgical Intraocular Pressure Reduction in Patients with Open-Angle Glaucoma. Clin Ophthalmol. 2021 Jul 14;15:3017-3026. doi: 10.2147/OPTH.S317190. eCollection 2021.
Results Reference
background
PubMed Identifier
24307717
Citation
Francoz M, Fenolland JR, Giraud JM, El Chehab H, Sendon D, May F, Renard JP. Reproducibility of macular ganglion cell-inner plexiform layer thickness measurement with cirrus HD-OCT in normal, hypertensive and glaucomatous eyes. Br J Ophthalmol. 2014 Mar;98(3):322-8. doi: 10.1136/bjophthalmol-2012-302242. Epub 2013 Dec 4.
Results Reference
background
PubMed Identifier
29934267
Citation
Lavinsky F, Wu M, Schuman JS, Lucy KA, Liu M, Song Y, Fallon J, de Los Angeles Ramos Cadena M, Ishikawa H, Wollstein G. Can Macula and Optic Nerve Head Parameters Detect Glaucoma Progression in Eyes with Advanced Circumpapillary Retinal Nerve Fiber Layer Damage? Ophthalmology. 2018 Dec;125(12):1907-1912. doi: 10.1016/j.ophtha.2018.05.020. Epub 2018 Jun 19.
Results Reference
background
PubMed Identifier
10892280
Citation
Klink T, Lieb WE, Gobel W. [Early and late findings with optical coherence tomography (OCT) in patients with postoperative hypotonia]. Ophthalmologe. 2000 May;97(5):353-8. doi: 10.1007/s003470050536. German.
Results Reference
background
PubMed Identifier
31554879
Citation
Kim WJ, Kim KN, Sung JY, Kim JY, Kim CS. Relationship between preoperative high intraocular pressure and retinal nerve fibre layer thinning after glaucoma surgery. Sci Rep. 2019 Sep 25;9(1):13901. doi: 10.1038/s41598-019-50406-7.
Results Reference
background
PubMed Identifier
28845126
Citation
Kadziauskiene A, Strelkauskaite E, Mockeviciute E, Asoklis R, Lesinskas E, Schmetterer L. Changes in macular thickness after trabeculectomy with or without adjunctive 5-fluorouracil. Acta Med Litu. 2017;24(2):93-100. doi: 10.6001/actamedica.v24i2.3489.
Results Reference
background
PubMed Identifier
22722487
Citation
Raghu N, Pandav SS, Kaushik S, Ichhpujani P, Gupta A. Effect of trabeculectomy on RNFL thickness and optic disc parameters using optical coherence tomography. Eye (Lond). 2012 Aug;26(8):1131-7. doi: 10.1038/eye.2012.115. Epub 2012 Jun 22.
Results Reference
background
PubMed Identifier
29663109
Citation
Silva D, Lopes AS, Henriques S, Lisboa M, Pinto S, Trancoso Vaz F, Prieto I. Changes in choroidal thickness following trabeculectomy and its correlation with the decline in intraocular pressure. Int Ophthalmol. 2019 May;39(5):1097-1104. doi: 10.1007/s10792-018-0918-y. Epub 2018 Apr 16.
Results Reference
background
PubMed Identifier
30363694
Citation
Diaconita V, Quinn M, Jamal D, Dishan B, Malvankar-Mehta MS, Hutnik C. Washout Duration of Prostaglandin Analogues: A Systematic Review and Meta-analysis. J Ophthalmol. 2018 Sep 27;2018:3190684. doi: 10.1155/2018/3190684. eCollection 2018.
Results Reference
background
PubMed Identifier
2678143
Citation
Mishima H, Masuda K, Miyake K. The putative role of prostaglandins in cystoid macular edema. Prog Clin Biol Res. 1989;312:251-64. No abstract available.
Results Reference
background
PubMed Identifier
8442684
Citation
Taheri PA, Karamanoukian H, Gibbons K, Waldman N, Doerr RJ, Hoover EL. Can patients with minor head injuries be safely discharged home? Arch Surg. 1993 Mar;128(3):289-92. doi: 10.1001/archsurg.1993.01420150043008.
Results Reference
background
PubMed Identifier
24222307
Citation
Gupta P, Sidhartha E, Tham YC, Chua DK, Liao J, Cheng CY, Aung T, Wong TY, Cheung CY. Determinants of macular thickness using spectral domain optical coherence tomography in healthy eyes: the Singapore Chinese Eye study. Invest Ophthalmol Vis Sci. 2013 Dec 5;54(13):7968-76. doi: 10.1167/iovs.13-12436.
Results Reference
background
PubMed Identifier
867638
Citation
Lichter PR. Variability of expert observers in evaluating the optic disc. Trans Am Ophthalmol Soc. 1976;74:532-72.
Results Reference
background
PubMed Identifier
32055953
Citation
Manabe K, Matsuoka Y, Tanito M. Incidence of macular edema development after filtration surgery. Graefes Arch Clin Exp Ophthalmol. 2020 Jun;258(6):1343-1345. doi: 10.1007/s00417-020-04624-9. Epub 2020 Feb 13. No abstract available.
Results Reference
background
PubMed Identifier
9098816
Citation
Belyea DA, Dan JA, Lieberman MF, Stamper RL. Midterm follow-up results of combined phacoemulsification, lens implantation, and mitomycin-C trabeculectomy procedure. J Glaucoma. 1997 Apr;6(2):90-8.
Results Reference
background
PubMed Identifier
24308226
Citation
Sesar A, Cavar I, Sesar AP, Geber MZ, Sesar I, Laus KN, Vatavuk Z, Mandic Z. Macular thickness after glaucoma filtration surgery. Coll Antropol. 2013 Sep;37(3):841-5.
Results Reference
background
PubMed Identifier
12644938
Citation
Karasheva G, Goebel W, Klink T, Haigis W, Grehn F. Changes in macular thickness and depth of anterior chamber in patients after filtration surgery. Graefes Arch Clin Exp Ophthalmol. 2003 Mar;241(3):170-5. doi: 10.1007/s00417-003-0628-6. Epub 2003 Feb 20.
Results Reference
background
PubMed Identifier
27588282
Citation
Pitale PM, Chatha U, Patel V, Gupta L, Waisbourd M, Pro MJ. Changes in macular thickness following glaucoma surgery. Int J Ophthalmol. 2016 Aug 18;9(8):1236-7. doi: 10.18240/ijo.2016.08.24. eCollection 2016. No abstract available.
Results Reference
background
PubMed Identifier
33880684
Citation
Demirtas AA, Karahan M, Erdem S, Aslan Kaya A, Keklikci U. Long-term effects of trabeculectomy in primary open-angle glaucoma on segmented macular ganglion cell complex alterations. Int Ophthalmol. 2021 Jun;41(6):2249-2263. doi: 10.1007/s10792-021-01840-y. Epub 2021 Apr 21.
Results Reference
background
PubMed Identifier
36147280
Citation
Nilforushan N, Loni S, Abdolalizadeh P, Miraftabi A, Banifatemi M, Rakhshan R, Jafari S, Abolfathzadeh N. Early Macular Thickness Changes after Trabeculectomy and Combined Phaco-Trabeculectomy. J Curr Ophthalmol. 2022 Jul 26;34(2):160-166. doi: 10.4103/joco.joco_333_21. eCollection 2022 Apr-Jun.
Results Reference
background
PubMed Identifier
36737088
Citation
Wagner FM, Schuster AK, Kianusch K, Stingl J, Pfeiffer N, Hoffmann EM. Long-term success after trabeculectomy in open-angle glaucoma: results of a retrospective cohort study. BMJ Open. 2023 Feb 3;13(2):e068403. doi: 10.1136/bmjopen-2022-068403.
Results Reference
background
PubMed Identifier
29870414
Citation
Koike KJ, Chang PT. Trabeculectomy: A Brief History and Review of Current Trends. Int Ophthalmol Clin. 2018 Summer;58(3):117-133. doi: 10.1097/IIO.0000000000000231. No abstract available.
Results Reference
background
PubMed Identifier
17181451
Citation
Hollo G. The side effects of the prostaglandin analogues. Expert Opin Drug Saf. 2007 Jan;6(1):45-52. doi: 10.1517/14740338.6.1.45.
Results Reference
background
PubMed Identifier
25328381
Citation
Alm A. Latanoprost in the treatment of glaucoma. Clin Ophthalmol. 2014 Sep 26;8:1967-85. doi: 10.2147/OPTH.S59162. eCollection 2014.
Results Reference
background
PubMed Identifier
15921747
Citation
van der Valk R, Webers CA, Schouten JS, Zeegers MP, Hendrikse F, Prins MH. Intraocular pressure-lowering effects of all commonly used glaucoma drugs: a meta-analysis of randomized clinical trials. Ophthalmology. 2005 Jul;112(7):1177-85. doi: 10.1016/j.ophtha.2005.01.042.
Results Reference
background
PubMed Identifier
30862377
Citation
Gazzard G, Konstantakopoulou E, Garway-Heath D, Garg A, Vickerstaff V, Hunter R, Ambler G, Bunce C, Wormald R, Nathwani N, Barton K, Rubin G, Buszewicz M; LiGHT Trial Study Group. Selective laser trabeculoplasty versus eye drops for first-line treatment of ocular hypertension and glaucoma (LiGHT): a multicentre randomised controlled trial. Lancet. 2019 Apr 13;393(10180):1505-1516. doi: 10.1016/S0140-6736(18)32213-X. Epub 2019 Mar 9. Erratum In: Lancet. 2019 Jul 6;394(10192):e1.
Results Reference
background
PubMed Identifier
15021220
Citation
Leske MC, Heijl A, Hyman L, Bengtsson B, Komaroff E. Factors for progression and glaucoma treatment: the Early Manifest Glaucoma Trial. Curr Opin Ophthalmol. 2004 Apr;15(2):102-6. doi: 10.1097/00055735-200404000-00008.
Results Reference
background
PubMed Identifier
26581556
Citation
Prum BE Jr, Rosenberg LF, Gedde SJ, Mansberger SL, Stein JD, Moroi SE, Herndon LW Jr, Lim MC, Williams RD. Primary Open-Angle Glaucoma Preferred Practice Pattern((R)) Guidelines. Ophthalmology. 2016 Jan;123(1):P41-P111. doi: 10.1016/j.ophtha.2015.10.053. Epub 2015 Nov 12. Erratum In: Ophthalmology. 2018 Jun;125(6):949.
Results Reference
background
PubMed Identifier
24825645
Citation
Weinreb RN, Aung T, Medeiros FA. The pathophysiology and treatment of glaucoma: a review. JAMA. 2014 May 14;311(18):1901-11. doi: 10.1001/jama.2014.3192.
Results Reference
background
PubMed Identifier
33881589
Citation
Schuster AK, Wagner FM, Pfeiffer N, Hoffmann EM. Risk factors for open-angle glaucoma and recommendations for glaucoma screening. Ophthalmologe. 2021 Jul;118(Suppl 2):145-152. doi: 10.1007/s00347-021-01378-5. Epub 2021 Apr 21.
Results Reference
background
PubMed Identifier
29032195
Citation
Flaxman SR, Bourne RRA, Resnikoff S, Ackland P, Braithwaite T, Cicinelli MV, Das A, Jonas JB, Keeffe J, Kempen JH, Leasher J, Limburg H, Naidoo K, Pesudovs K, Silvester A, Stevens GA, Tahhan N, Wong TY, Taylor HR; Vision Loss Expert Group of the Global Burden of Disease Study. Global causes of blindness and distance vision impairment 1990-2020: a systematic review and meta-analysis. Lancet Glob Health. 2017 Dec;5(12):e1221-e1234. doi: 10.1016/S2214-109X(17)30393-5. Epub 2017 Oct 11.
Results Reference
background
PubMed Identifier
33275949
Citation
GBD 2019 Blindness and Vision Impairment Collaborators; Vision Loss Expert Group of the Global Burden of Disease Study. Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to VISION 2020: the Right to Sight: an analysis for the Global Burden of Disease Study. Lancet Glob Health. 2021 Feb;9(2):e144-e160. doi: 10.1016/S2214-109X(20)30489-7. Epub 2020 Dec 1. Erratum In: Lancet Glob Health. 2021 Apr;9(4):e408.
Results Reference
background
Links:
URL
https://cerof.ufg.br
Description
Centro de Referencia em Oftalmologia
Available IPD and Supporting Information:
Available IPD/Information Type
Informed Consent Form
Available IPD/Information URL
http://repositorio.bc.ufg.br
Available IPD/Information Identifier
Repositorio
Available IPD/Information Comments
Repositorio da Biblioteca Central da Universidade Federal de Goias

Learn more about this trial

Evaluation of Retina in Patients With Glaucoma Using Topical Prostaglandins Undergoing Trabeculectomy Surgery

We'll reach out to this number within 24 hrs