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NCT00571896 · ClinicalTrials.gov registry record · Phase 2
The Use of SennaS for Prevention of Post-operative Constipation After Urogynecologic Surgery
A Phase 2 study, sponsored by Hartford Hospital.
- Completed
- Registry status
- Phase 2
- Development phase
- 72
- Enrollment target
NCT00571896 is a Phase 2 study that has completed, run by Hartford Hospital. The registered enrollment target is 72 participants.
The verdict
NCT00571896, a Phase 2 study, has completed, sponsored by Hartford Hospital.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 72 participants
- Enrollment target
Study Summary
We are doing this study to see if using an over the counter mild laxative, SennaS, there is a difference in time required to have a bowel movement in women who are having surgery for prolapse (when your uterus and/or vagina drop after childbirth or with age) and/or incontinence (when you leak urine or stool without your control) as compared to a sugar pill or placebo.
Interventions
- DRUG placebo
- DRUG Senna+ docusate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2008-01 |
| Est. Completion | 2009-06 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00571896
The ClinicalTrials.gov registry entry for NCT00571896 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hartford Hospital, which has 75 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.
NCT00571896 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00571896 about?
NCT00571896 is a clinical study titled "The Use of SennaS for Prevention of Post-operative Constipation After Urogynecologic Surgery". We are doing this study to see if using an over the counter mild laxative, SennaS, there is a difference in time required to have a bowel movement in women who are having surgery for prolapse (when your uterus and/or vagina drop after childbirth or with age) and/or incontinence (when you leak urine ...
What is the current status of trial NCT00571896?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 72 participants. The study started on 2008-01. Estimated completion is 2009-06.
What interventions are being tested in trial NCT00571896?
The interventions under investigation include: placebo (DRUG), Senna+ docusate (DRUG).
Who is sponsoring clinical trial NCT00571896?
This trial is sponsored by Hartford Hospital, which has 75 total clinical trials registered on ClinicalTrials.gov.
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