Ileus Postoperative

5

Review clinical trials related to Ileus Postoperative. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Oral Lactulose for Gastrointestinal Recovery After Complex Appendectomy

This is a prospective, triple-blind, placebo-controlled, single-center randomized clinical trial to evaluate the efficacy and safety of early oral lactulose for promoting postoperative gastrointestinal functional recovery in patients undergoing appendectomy for complicated appendicitis. Eligible patients aged ≥18 years with complicated appendicitis confirmed by preoperative SAS 2.0 score, intraoperative findings, or postoperative pathology will be randomly assigned 1:1 to receive oral lactulose or placebo on postoperative day 1 and day 2. The primary outcome is time to GI-2 (time from surgery to the later of first defecation or first tolerance of solid food). Secondary outcomes include time to first flatus, defecation rate within 72 hours, postoperative nausea and vomiting, length of hospital stay, medical costs, postoperative complications, and lactulose-related adverse events. A total of 150 patients will be enrolled. This study aims to provide high-level evidence for optimizing postoperative management in patients with complicated appendicitis.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Nanchong Central HospitalUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

1.Age ≥18 years.2.Complicated appendicitis confirmed by SAS2.0 score, intraopera...

1.Preoperative intestinal obstruction, IBD, or intestinal tumor.2.Planned postop...

Status: Not yet recruiting

The ACURE Trial: Acupuncture for Colorectal Recovery

Purpose: The goal of this clinical trial is to evaluate whether electroacupuncture (EA) can accelerate the recovery of bowel function in patients undergoing minimally invasive surgery for colorectal cancer. Main Questions to be Answered: Does electroacupuncture reduce the time to the first bowel movement after surgery compared to standard care or a "sham" (placebo) treatment? Can electroacupuncture improve overall gastrointestinal tolerance and reduce postoperative discomfort? Study Design: Participants will be randomly assigned to one of three groups: Electroacupuncture Group: Receives active electrical stimulation at specific acupuncture points. Sham Acupuncture Group: Receives superficial needling at non-treatment points with no electrical current to serve as a placebo. Standard Care Group: Receives standard hospital recovery protocols (ERAS) without acupuncture. All treatments will consist of four 30-minute sessions: one before surgery and three on the days following the procedure. Researchers will compare the three groups to see if the electroacupuncture group experiences a faster return of digestive function.

Participants needed: 240
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Chang Gung Memorial HospitalUpdated: Apr 6, 2026
Eligibility criteria

Histologically confirmed colorectal cancer requiring scheduled curative-intent r... [+3]

Pregnant or breastfeeding women. [+13]

Status: Recruiting

Effect of Lollipop on Postoperative Gastrointestinal Recovery in Children

Postoperative ileus is common in children. There are various method to prevent postoperative ileus. In this study, the investigators will explore the role of sucking lollipop after operation on the recovery of gastrointestinal function in children.

Participants needed: 50
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: The University of Hong KongUpdated: Dec 11, 2024Locations: 1
Eligibility criteria

Patients receiving major abdominal surgery (e.g.appendicectomy, choledochal cyst...

Patients with neurological conditions that preclude sucking/swallowing. [+2]

Status: Recruiting

Preventing Gastrointestinal Disturbance in Patients After Longitudinal Laparotomy.

This is a multi-center, randomized, double blind, placebo-controlled, phase 2 pilot efficacy study.

Participants needed: 126
Trial details
Phase: Phase 2Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Orexa BVUpdated: Oct 3, 2024Locations: 3
Eligibility criteria

Patient must be able to understand the requirements of the study and give writte... [+5]

Patient has a history of gastrectomy, total colectomy, stoma creation, short bow... [+15]

Status: Recruiting

Time to Return of Bowel Function Following Perioperative Probiotics in Colorectal Cancer Surgery

There is pre-existing evidence that probiotics could be useful in the improvement of ileus rates. One metaanalysis of 30 studies demonstrated a reduction in the prevalence of post-operative ileus as determined by time to flatus, time to defecation, as well as postoperative abdominal distension (PMID:37373843). More broadly in gastrointestinal surgery, a meta-analysis of 21 randomised controlled trials similarly affirmed the speedier recovery of gastrointestinal function after surgery when probiotics were administered (PMID: 35231076). In spite of these advantages, the routine use of probiotics perioperatively for colorectal cancer surgery is not performed in Singapore. We therefore seek to perform a trial to investigate whether probiotic administration perioperatively may reduce post operative ileus rates.

Participants needed: 162
Trial details
Age: 21-99Biological sex: AllType: InterventionalSponsor: National University Hospital, SingaporeUpdated: Jun 13, 2024Locations: 1
Eligibility criteria

undergoing elective colorectal cancer surgery in which an oncologic resection is... [+4]

patients with known contraindications to probiotic use [+4]