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NCT03523715 · ClinicalTrials.gov registry record · Phase 4
Prunes for Gastrointestinal Function After Gynecologic Surgery
A Phase 4 study, sponsored by University of Southern California.
- Terminated
- Registry status
- Phase 4
- Development phase
- 77
- Enrollment target
NCT03523715 is a Phase 4 study that was terminated before completion, run by University of Southern California. The registered enrollment target is 77 participants.
The verdict
NCT03523715, a Phase 4 study, was terminated before completion, sponsored by University of Southern California.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 77 participants
- Enrollment target
Study Summary
This is a prospective, randomized control trial that randomizes patients post-operatively into standard care versus standard care plus prunes. Patients in the control arm will take 100 mg docusate twice per day for 3 days (standard care). Participants in the treatment arm will consume 4 oz prunes daily and take 100 mg docusate twice per day for 3 days. The primary objective is to determine the time to first bowel movement after surgery.
Interventions
- DIETARY_SUPPLEMENT Prunes
- DRUG Docusate Sodium
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 77 participants |
| Start Date | 2017-11-30 |
| Est. Completion | 2020-07-31 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03523715
The ClinicalTrials.gov registry entry for NCT03523715 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 77 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Southern California, which has 617 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Prunes is the first listed.
NCT03523715 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03523715 about?
NCT03523715 is a clinical study titled "Prunes for Gastrointestinal Function After Gynecologic Surgery". This is a prospective, randomized control trial that randomizes patients post-operatively into standard care versus standard care plus prunes. Patients in the control arm will take 100 mg docusate twice per day for 3 days (standard care). Participants in the treatment arm will consume 4 oz prunes da...
What is the current status of trial NCT03523715?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 77 participants. The study started on 2017-11-30. Estimated completion is 2020-07-31.
What interventions are being tested in trial NCT03523715?
The interventions under investigation include: Prunes (DIETARY_SUPPLEMENT), Docusate Sodium (DRUG).
Who is sponsoring clinical trial NCT03523715?
This trial is sponsored by University of Southern California, which has 617 total clinical trials registered on ClinicalTrials.gov.
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