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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
Kocatepe University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Benign Prostatic Hyperplasia

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

    First Posted
    May 2, 2017
    Last Updated
    May 4, 2017
    Sponsor
    Kocatepe University
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    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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