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NCT01393171 · ClinicalTrials.gov registry record · NA
Anterior Colporrhaphy Versus Cystocele Repair Using Polypropylene Mesh or Porcine Dermis
A NA study, sponsored by Kaiser Permanente.
- Completed
- Registry status
- NA
- Development phase
- 99
- Enrollment target
NCT01393171 is a NA study that has completed, run by Kaiser Permanente. The registered enrollment target is 99 participants.
The verdict
NCT01393171, a NA study, has completed, sponsored by Kaiser Permanente.
- COMPLETED
- Registry status
- NA
- Development phase
- 99 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the success rate of cystocele repair using polypropylene mesh or porcine dermis compared to that of anterior colporrhaphy in a prospective randomized fashion. The study will be performed in a randomized, prospective, single-blinded fashion.
Interventions
- DEVICE Polypropylene mesh (Polyform by Boston Scientific)
- PROCEDURE Porcine Dermis (Pelvicol by CRBard)
- PROCEDURE Anterior Colporrhaphy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 99 participants |
| Start Date | 2006-01 |
| Est. Completion | 2018-04-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01393171
The ClinicalTrials.gov registry entry for NCT01393171 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 99 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kaiser Permanente, which has 294 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Polypropylene mesh (Polyform by Boston Scientific) is the first listed.
NCT01393171 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01393171 about?
NCT01393171 is a clinical study titled "Anterior Colporrhaphy Versus Cystocele Repair Using Polypropylene Mesh or Porcine Dermis". The purpose of this study is to evaluate the success rate of cystocele repair using polypropylene mesh or porcine dermis compared to that of anterior colporrhaphy in a prospective randomized fashion. The study will be performed in a randomized, prospective, single-blinded fashion.
What is the current status of trial NCT01393171?
This trial is currently completed. It is a NA study. The enrollment target is 99 participants. The study started on 2006-01. Estimated completion is 2018-04-01.
What interventions are being tested in trial NCT01393171?
The interventions under investigation include: Polypropylene mesh (Polyform by Boston Scientific) (DEVICE), Porcine Dermis (Pelvicol by CRBard) (PROCEDURE), Anterior Colporrhaphy (PROCEDURE).
Who is sponsoring clinical trial NCT01393171?
This trial is sponsored by Kaiser Permanente, which has 294 total clinical trials registered on ClinicalTrials.gov.
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