Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
40 participants
INTERVENTIONAL
2017-01-01
2018-03-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Abdominal Versus Vaginal Hysteropexy
NCT03494582
Abdominal Sacral Hysteropexy Versus Vaginal Sacrospinous Hysteropexy
NCT04850365
Laparoscopic Ventral Mesh Rectopexy Versus Trans-vaginal Repair for Anterior Rectocele.
NCT06633172
Study Comparing Transobturator Cystocele vs. Anterior Vaginal RepairS
NCT05602246
Modified Purandare's Cervicopexy Versus Abdominal Sacral Hysteropexy
NCT04852991
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Transobturator arm
Transobturator Paravaginal Repair
Transobturator Paravaginal Repair
Transobturator application of sutures to the white line in cases needing paravaginal repair
Transvaginal arm
traditional transvaginal Paravaginal Repair
traditional transvaginal Paravaginal Repair
traditional transvaginal application of sutures to the white line
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Transobturator Paravaginal Repair
Transobturator application of sutures to the white line in cases needing paravaginal repair
traditional transvaginal Paravaginal Repair
traditional transvaginal application of sutures to the white line
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
midline and paravaginal defect cystocele
Exclusion Criteria
20 Years
50 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ain Shams Maternity Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hamdy Ahmed Saaid
Fellow of obstetrics & gynecology
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Hamdy HA Saaid, MD
Role: PRINCIPAL_INVESTIGATOR
Ain Shams University
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TVTOPVR
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.