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NCT01911793 · ClinicalTrials.gov registry record · NA
Stoma Tube Decompression and Postoperative Ileus After Major Colorectal Surgery
A NA study, sponsored by Cedars-Sinai Medical Center.
- Terminated
- Registry status
- NA
- Development phase
- 6
- Enrollment target
NCT01911793 is a NA study that was terminated before completion, run by Cedars-Sinai Medical Center. The registered enrollment target is 6 participants.
The verdict
NCT01911793, a NA study, was terminated before completion, sponsored by Cedars-Sinai Medical Center.
- TERMINATED
- Registry status
- NA
- Development phase
- 6 participants
- Enrollment target
Study Summary
Postoperative ileus is common after colorectal surgery, occurring in up to 20% of patients. Stomas are frequently created in conjunction with major colorectal surgery. Obstruction at the level of the stoma is a common cause of bowel obstruction or ileus. This is often manifested by decrease or delay in stoma output and is often attributed to edema at the level of the stoma. Thus, a temporary tube (red robinson catheter) is placed into the stoma at bedside, which often relieves the obstruction until the edema at the level of the stoma resolves and stoma function occurs around the temporary tube. At this time, the tube is removed and the stoma continues to function normally. The purpose of this study is to evaluate whether a stoma tube (red-robinson catheter) placed at the time of stoma creation would reduce the incidence of postoperative ileus in patients undergoing major colorectal surgery with creation of a stoma.
Interventions
- DEVICE Stoma Tube
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 6 participants |
| Start Date | 2013-07 |
| Est. Completion | 2014-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01911793
The ClinicalTrials.gov registry entry for NCT01911793 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cedars-Sinai Medical Center, which has 339 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Stoma Tube is the first listed.
NCT01911793 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01911793 about?
NCT01911793 is a clinical study titled "Stoma Tube Decompression and Postoperative Ileus After Major Colorectal Surgery". Postoperative ileus is common after colorectal surgery, occurring in up to 20% of patients. Stomas are frequently created in conjunction with major colorectal surgery. Obstruction at the level of the stoma is a common cause of bowel obstruction or ileus. This is often manifested by decrease or delay...
What is the current status of trial NCT01911793?
This trial is currently terminated. It is a NA study. The enrollment target is 6 participants. The study started on 2013-07. Estimated completion is 2014-07.
What interventions are being tested in trial NCT01911793?
The interventions under investigation include: Stoma Tube (DEVICE).
Who is sponsoring clinical trial NCT01911793?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
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