The Effects of α-adrenergic Receptor Antagonists on Choroid and Pupil
Primary Purpose
Benign Prostatic Hyperplasia, Pupil Anomaly, Choroid Disease
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Alfuzosin Hydrochloride 10 MG
Tamsulosin Hydrochloride 0.4 MG
Sponsored by
About this trial
This is an interventional treatment trial for Benign Prostatic Hyperplasia
Eligibility Criteria
Inclusion Criteria:
- Best corrected visual acuity (BCVA) ≥ 0.8
- Diagnosis of BPH and initiation of alfuzosin hydrochloride or tamsulosin hydrochloride treatments
- 45 years of age or older man
Exclusion Criteria:
- Occluded angle by gonioscopy (grade 0, narrow angle, grade I, grade II)
- Corneal scarring or cataract that prevents appearance of the fundus
- Formation of macular or peripheral retinal pathologies or choroidopathy
- Optic nerve pathologies such as optic neuropathy
- Spherical refractive error ≥ ±6.00 D or cylinder refractive error ≥ ±3.00 D
- Systemic diseases that may affect choroidal blood flow
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Alfuzosin Hydrochloride
Tamsulosin Hydrochloride
Arm Description
Alfuzosin hydrochloride 10 mg tablet by mouth, every 24 hours for 3 months
Tamsulosin hydrochloride 0.4 mg tablet by mouth, every 24 hours for 3 months
Outcomes
Primary Outcome Measures
Change from baseline choroidal thicknesses at 3 months
Choroidal thicknesses (CTs) measurement under the fovea, 3 mm nasal to the fovea and 3 mm temporal to the fovea at baseline, 1st and 3rd month, and recording as submacular (SCT), nasal (NCT) and temporal (TCT) choroidal thicknesses.
Change from baseline pupil diameter sizes at 3 months
Mesopic, scotopic and photopic pupil diameter sizes measurement at baseline, 1st and 3rd months
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03144596
Brief Title
The Effects of α-adrenergic Receptor Antagonists on Choroid and Pupil
Official Title
The Effects of Systemic Alfuzosin and Tamsulosin Hydrochloride on Choroidal Thickness and Pupil Diameter Sizes in Cases With Benign Prostatic Hyperplasia
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
October 29, 2015 (Actual)
Primary Completion Date
February 3, 2016 (Actual)
Study Completion Date
November 19, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kocatepe University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
It was aimed to evaluate and investigate the effects of tamsulosin hydrochloride, has preferential selectivity for the α1A receptor in the prostat versus the α1B receptor in the blood vessels, and alfuzosin hydrochloride on choroidal thickness (CT), pupil diameter sizes evaluated by using enhanced depth imaging spectral-domain optical coherence tomography (EDI-OCT) and scheimpflug/placido photography-based topoghraphy system in this study.
63 men patients with newly diagnosis of benign prostatic hyperplasia were randomly assigned to either alfuzosin hydrochloride or to tamsulosin hydrochloride groups in this prospective, randomized, parallel-group clinical trial. Enhanced depth imaging spectral-domain optical coherence tomography, pupillography were obtained at baseline, 1st and 3rd month, and choroidal thicknesses and pupil diameter sizes were compared between the 2 groups.
Detailed Description
The local authorized clinical trials ethics committee approved the study and this study was performed following the principles of the Declaration of Helsinki. Detailed information was given to patients about clinical applications and tests, and signed informed consent forms were also obtained from all patients. 32 right eyes of 32 men with diagnosis of BPH initiated on AH (Xatral®) (10 mg/day) and 31 right eyes of 31 men with diagnosis of BPH initiated on TH (Flomax®) (0.4 mg/day) were included in this self-controlled prospective clinical trial. Urologists in the urology clinic made diagnosis of BPH, and 63 men diagnosis of BPH were directed towards eye clinic. AH or TH treatments were randomly recommended for previously untreated patients with newly diagnosis of BPH by urologists. After providing information to patients about the disease and treatment, patients predicted to show adherence to treatment, were enrolled in the study.
Ophthalmological examinations were performed in all cases. Choroidal thicknesses (CTs) were measured under the fovea, 3 mm nasal to the fovea and 3 mm temporal to the fovea, and they were recorded as submacular (SCT), nasal (NCT) and temporal (TCT) choroidal thicknesses. CTs were measured and recorded by using EDI-OCT imaging (Cirrus HD 4000, Carl Zeis Meditec, CA, USA). Mesopic, scotopic and photopic pupil diameter sizes were measured and recorded by using Scheimpflug/Placido photography-based topography system in the pupillometer mode (Sirius, Italy). CTs, scotopic, mesopic and photopic pupil diameter sizes were measured and recorded at baseline, 1st and 3rd months.
Data obtained from cases were encoded and they were transferred to the computer program. SPSS 20.0 software (SPSS Inc., Chicago, IL, USA) was used for statistical evaluation. Data distribution was tested using Kolmogorov-Smirnov test. Baseline values and 1st, 3rd month values were compared by using the repeated measure of ANOVA in intra-group evaluation and independent samples t-test in inter-group evaluation, and the significance level of p-value was accepted as 0,05 (P ≤ 0, 05). Progressions were evaluated by using repeated measures analyses of variance-ANOVA (with the Bonferroni correction) and the correlation between parameters were evaluated by using bivariate (Pearson's) correlation analysis. Positive values and negative values were considered to be correlated in the same direction and opposite direction, respectively in correlation analysis. Correlation coefficient values r ≥ |± 0.3| were accepted as correlation; and the significance level of P value that was below 0,05 was evaluated as the significant correlation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostatic Hyperplasia, Pupil Anomaly, Choroid Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
prospective, randomized, parallel-group clinical trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
63 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Alfuzosin Hydrochloride
Arm Type
Experimental
Arm Description
Alfuzosin hydrochloride 10 mg tablet by mouth, every 24 hours for 3 months
Arm Title
Tamsulosin Hydrochloride
Arm Type
Active Comparator
Arm Description
Tamsulosin hydrochloride 0.4 mg tablet by mouth, every 24 hours for 3 months
Intervention Type
Drug
Intervention Name(s)
Alfuzosin Hydrochloride 10 MG
Other Intervention Name(s)
Xatral
Intervention Description
Alfuzosin hydrochloride Tablet
Intervention Type
Drug
Intervention Name(s)
Tamsulosin Hydrochloride 0.4 MG
Other Intervention Name(s)
Flomax
Intervention Description
Tamsulosin Hydrochloride Tablet
Primary Outcome Measure Information:
Title
Change from baseline choroidal thicknesses at 3 months
Description
Choroidal thicknesses (CTs) measurement under the fovea, 3 mm nasal to the fovea and 3 mm temporal to the fovea at baseline, 1st and 3rd month, and recording as submacular (SCT), nasal (NCT) and temporal (TCT) choroidal thicknesses.
Time Frame
1 month and 2 months
Title
Change from baseline pupil diameter sizes at 3 months
Description
Mesopic, scotopic and photopic pupil diameter sizes measurement at baseline, 1st and 3rd months
Time Frame
1 month and 2 months
10. Eligibility
Sex
Male
Gender Based
Yes
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Best corrected visual acuity (BCVA) ≥ 0.8
Diagnosis of BPH and initiation of alfuzosin hydrochloride or tamsulosin hydrochloride treatments
45 years of age or older man
Exclusion Criteria:
Occluded angle by gonioscopy (grade 0, narrow angle, grade I, grade II)
Corneal scarring or cataract that prevents appearance of the fundus
Formation of macular or peripheral retinal pathologies or choroidopathy
Optic nerve pathologies such as optic neuropathy
Spherical refractive error ≥ ±6.00 D or cylinder refractive error ≥ ±3.00 D
Systemic diseases that may affect choroidal blood flow
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mustafa Dogan, Asst. Prof.
Organizational Affiliation
Afyon Kocatepe University Eye Clinics
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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The Effects of α-adrenergic Receptor Antagonists on Choroid and Pupil
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