Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01559662 · ClinicalTrials.gov registry record · NA
Effect of Sugared Chewing Gum on Gastrointestinal Recovery After Major Colorectal Surgery
A NA study of Postoperative Ileus, sponsored by Cedars-Sinai Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 114
- Enrollment target
- 1
- Study location
NCT01559662: Completed NA study of Postoperative Ileus, sponsored by Cedars-Sinai Medical Center.
NCT01559662 is a NA study of Postoperative Ileus that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 114 participants, above the 73-participant average among 3 other Postoperative Ileus trials with a reported enrollment target (56% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01559662, a NA study of Postoperative Ileus, has completed, sponsored by Cedars-Sinai Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 114 participants
- Enrollment target
- 1
- Study location
Study Summary
The Purpose of this study is to evaluate the effect of gum chewing on recovery of gastrointestinal function in patient undergoing major colorectal surgery. The investigators hypothesize that patients who chew gum after major colorectal surgery will have faster recovery of gastrointestinal function.
Primary Outcome
Time measured from end of operation to patient tolerating 50% of a low residue diet without emesis in 24 hours
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Sugared Chewing Gum (Juicy Fruit)
Study Locations (1)
California
- Cedars Sinai Medical Center - Los Angeles
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 114 participants |
| Start Date | 2010-08 |
| Est. Completion | 2012-03 |
| Phase | NA |
What the finished NCT01559662 record still lists
NCT01559662 is an interventional study that assigns participants to a tested intervention. The registered 114 participants enrollment target is mid-sized for trials with a published cap, above the 73-participant average among 3 other Postoperative Ileus trials with a reported enrollment target (56% higher).
The record links to 1 condition, with Postoperative Ileus appearing as the primary indexed condition, and to 1 intervention - of which Sugared Chewing Gum (Juicy Fruit) is the first listed.
NCT01559662 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT01559662 about?
NCT01559662 is a clinical study titled "Effect of Sugared Chewing Gum on Gastrointestinal Recovery After Major Colorectal Surgery". The Purpose of this study is to evaluate the effect of gum chewing on recovery of gastrointestinal function in patient undergoing major colorectal surgery. The investigators hypothesize that patients who chew gum after major colorectal surgery will have faster recovery of gastrointestinal function.
What is the current status of trial NCT01559662?
This trial is currently completed. It is a NA study. The enrollment target is 114 participants. The study started on 2010-08. Estimated completion is 2012-03.
What conditions does trial NCT01559662 study?
This clinical trial studies the following conditions: Postoperative Ileus.
What interventions are being tested in trial NCT01559662?
The interventions under investigation include: Sugared Chewing Gum (Juicy Fruit) (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT01559662?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01559662 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postoperative Ileus
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT04522791 · 114 participants · Phase 2
Breathing, Relaxation, Attention Training, & Health in Older Adults (BREATHE)
- NCT04875052 · 114 participants · NA
Vibration and Post-traumatic Osteoarthritis Risk Following ACL Injury
- NCT05100342 · 114 participants
Prospective Validation of a Points Score System Predicting 30-day Survival
- NCT05224089 · 114 participants · Phase 4
Bilateral TAP and RS Blocks Using Liposomal Bupivacaine/Bupivacaine vs. Regular Bupivacaine in Laparoscopic Colectomy
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia