Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT03658395 · ClinicalTrials.gov registry record · NA
Sacrocolpopexy With Posterior Repair Obstructed Defecation Symptoms
A NA study, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT03658395 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 60 participants.
The verdict
NCT03658395, a NA study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
Participants who undergo laparoscopic sacrocolpopexy (LSCP) plus posterior repair (PR) will demonstrate greater improvement bowel symptom scores compared to participants who undergo LSCP alone at 3 months postoperatively.
Interventions
- PROCEDURE Laparoscopic Sacrocolopopexy
- PROCEDURE Posterior repair
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2018-07-19 |
| Est. Completion | 2024-04-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03658395
The ClinicalTrials.gov registry entry for NCT03658395 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Laparoscopic Sacrocolopopexy is the first listed.
NCT03658395 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03658395 about?
NCT03658395 is a clinical study titled "Sacrocolpopexy With Posterior Repair Obstructed Defecation Symptoms". Participants who undergo laparoscopic sacrocolpopexy (LSCP) plus posterior repair (PR) will demonstrate greater improvement bowel symptom scores compared to participants who undergo LSCP alone at 3 months postoperatively.
What is the current status of trial NCT03658395?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2018-07-19. Estimated completion is 2024-04-01.
What interventions are being tested in trial NCT03658395?
The interventions under investigation include: Laparoscopic Sacrocolopopexy (PROCEDURE), Posterior repair (PROCEDURE).
Who is sponsoring clinical trial NCT03658395?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.