Gastrointestinal Motility

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

Condition / disease
Location
Status: Recruiting

Effects of Electroacupuncture at NP82 and SP15 on Bowel Motility in Healthy Subjects

This study aims to investigate how a specific combination of electroacupuncture points, Tongbian (NP82) and Daheng (SP15), affects bowel movements in healthy volunteers. Constipation is a significant health issue, especially for post-stroke patients, and current treatments like laxatives often have unwanted side effects. The researchers want to determine if stimulating these two acupuncture points can objectively increase the frequency of bowel activity. Participants will undergo a three-stage procedure: a 30-minute period of baseline bowel sound recording, followed by 20 minutes of electroacupuncture stimulation at the specific points, and a final 30-minute recording period after the intervention. Throughout the study, an advanced digital stethoscope (3M™ Littmann® CORE) will be used to record bowel sounds objectively. This data will then be analyzed to measure any significant changes in bowel motility caused by the acupuncture.

Participants needed: 30
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: University of Medicine and Pharmacy at Ho Chi Minh CityUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Healthy volunteers aged 18 years and older. [+6]

Participants with severe medical conditions (heart, brain, liver, kidney, hemato... [+6]

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

Effects of Mobilization and Caffeine After Cesarean

This study Maims to assess bowel motility, pain and psychological well-being in women in the post-cesarean period by mobilizing them early and encouraging them to consume coffee.

Participants needed: 60
Trial details
Age: 18-35Biological sex: FemaleType: InterventionalSponsor: KTO Karatay UniversityUpdated: Feb 9, 2026Locations: 1
Eligibility criteria

Being between 18 and 35 years of age, [+3]

Women who underwent emergency cesarean delivery, [+13]

Status: Not yet recruiting

Hot Water Foot Bath for Pain and Gas Relief After Laparoscopic Cholecystectomy

This study investigates the effects of a hot foot bath on postoperative pain and time to first gas release in patients undergoing laparoscopic cholecystectomy. The intervention is a non-pharmacological supportive method applied during the early postoperative period. Participants will be randomly assigned to either intervention or control groups. No FDA-regulated drug or device is involved.

Participants needed: 62
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Cansu MertUpdated: Dec 5, 2025Locations: 1
Eligibility criteria

Age 18 years or older [+6]

Undergoing emergency cholecystectomy or open surgery (laparotomy) [+5]