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NCT00065234 · ClinicalTrials.gov registry record · Phase 2
Acupuncture to Prevent Postoperative Bowel Paralysis (Paralytic Ileus)
A Phase 2 study, sponsored by National Center for Complementary and Integrative Health (NCCIH).
- Terminated
- Registry status
- Phase 2
- Development phase
- 100
- Enrollment target
NCT00065234 is a Phase 2 study that was terminated before completion, run by National Center for Complementary and Integrative Health (NCCIH). The registered enrollment target is 100 participants.
The verdict
NCT00065234, a Phase 2 study, was terminated before completion, sponsored by National Center for Complementary and Integrative Health (NCCIH).
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 100 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if acupuncture is effective in preventing prolonged postoperative paralysis of the gastrointestinal tract among patients undergoing colostomy/ileostomy closure.
Interventions
- PROCEDURE Acupuncture
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2003-09 |
| Est. Completion | 2006-05 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00065234
The ClinicalTrials.gov registry entry for NCT00065234 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Center for Complementary and Integrative Health (NCCIH), which has 203 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Acupuncture is the first listed.
NCT00065234 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00065234 about?
NCT00065234 is a clinical study titled "Acupuncture to Prevent Postoperative Bowel Paralysis (Paralytic Ileus)". The purpose of this study is to determine if acupuncture is effective in preventing prolonged postoperative paralysis of the gastrointestinal tract among patients undergoing colostomy/ileostomy closure.
What is the current status of trial NCT00065234?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2003-09. Estimated completion is 2006-05.
What interventions are being tested in trial NCT00065234?
The interventions under investigation include: Acupuncture (PROCEDURE).
Who is sponsoring clinical trial NCT00065234?
This trial is sponsored by National Center for Complementary and Integrative Health (NCCIH), which has 203 total clinical trials registered on ClinicalTrials.gov.
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