Actively Recruiting
The Effect of Hot Compress Applied on the Intestines on Postoperative Nausea-vomiting and Bowel Function in Abdominal Surgery
Led by TC Erciyes University · Updated on 2025-10-06
80
Participants Needed
1
Research Sites
1 weeks
Total Duration
On this page
Sponsors
T
TC Erciyes University
Lead Sponsor
K
Kirsehir Ahi Evran Universitesi
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the effect of applying a hot compress to the intestines during abdominal surgery on postoperative nausea, vomiting, and bowel function. This randomized study involves patients undergoing abdominal surgery who meet specific criteria such as age and body mass index (BMI). The study aims to determine whether covering the intestines with saline heated to 36°C during surgery affects recovery outcomes like nausea and bowel function. Participants are randomly assigned to one of two groups. The intervention group will have their intestines covered with sterile gauze soaked in saline heated to 36°C during surgery to prevent drying and reduce infection risk. The control group will receive standard care, with intestines covered using gauze soaked in unheated saline. Both groups will undergo routine preoperative and postoperative procedures. Initially, 30 patients per group will be included, with further enrollment based on power analysis. Throughout the study, participants will complete forms and scales including the Patient Introduction Form, Patient Follow-up Form, Quality of Recovery-15 Scale (QoR-15), and Gastrointestinal Symptom Rating Scale (GSRS). Researchers will monitor gastrointestinal function by measuring time to first gas passage, first bowel movement, first normal bowel sounds, and first intake of liquid or semi-solid food. Postoperative gastrointestinal symptoms such as nausea, bloating, pain, and vomiting will also be assessed. The study will continue until early 2026, with careful monitoring of recovery and symptom severity.
CONDITIONS
Brief Title
Hot Compress Application in Open Abdominal Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Undergoing abdominal surgery in the general surgery ward
- 18 years of age or older
- Body mass index (BMI) between 18.50 and 24.99 kg/m²
- Able to communicate verbally
- Willing to participate in the study
- Conscious and oriented patients
You will not qualify if you...
- Previous gastrointestinal system surgery
- Postoperative complications
- History of small bowel resection, ileostomy, or colostomy
- History of inflammatory bowel disease, emergency surgery, neoadjuvant therapy, or appendectomy
- Chronic opioid use
- Chronic constipation with two or fewer bowel movements per week
- History of abdominal radiotherapy
- Admission to intensive care unit or postoperative bleeding
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Surgery day plus immediate post-operative period
Participants undergo abdominal surgery during which the intestines are covered with a sterile towel soaked in 36°C heated saline to prevent drying and reduce infection risk for the intervention group, or receive standard surgical care for the control group.
1 surgical visit
Duration - Postoperative 1 to 3 days
Participants are monitored for gastrointestinal function recovery including time to first passing gas, first defecation, first normal bowel sounds, and first consumption of liquid/semi-solid foods during the first 1 to 3 days after surgery.
Daily visits for up to 3 days after surgery
Trial Site Locations
Total: 1 location
1
Kırşehir Ahi Evran University
Merkez, Kırşehir, Turkey (Türkiye)
Actively Recruiting
Research Team
D
Dilek TALHAOĞLU, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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