Gastrointestinal Surgery

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

Condition / disease
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Status: Not yet recruiting

Preoperative Oral Carbohydrate Loading in Patients With Type 2 Diabetes Undergoing Gastrointestinal Surgery

This study is a single-center randomized controlled trial in adults with type 2 diabetes who are scheduled for elective gastrointestinal surgery. The study aims to find out whether drinking a carbohydrate-containing clear liquid before surgery can reduce early postoperative insulin resistance and improve blood glucose stability without increasing the risk of high or low blood glucose. Participants will be randomly assigned in a 1:1:1 ratio to one of three groups. The first group will receive standard enhanced recovery after surgery (ERAS) fasting and clear-fluid management without a carbohydrate-containing drink. The second group will drink 400 mL of a 12.5% maltodextrin carbohydrate solution, providing about 50 g of carbohydrate, approximately 2 hours before anesthesia. The third group will receive 500 mL of 10% glucose solution intravenously over approximately 2 hours before anesthesia. The intravenous glucose group is included mainly to help explore whether the route of carbohydrate administration affects the metabolic response. All participants will receive standard perioperative care. Blood glucose will be monitored during the perioperative period, including continuous glucose monitoring when available, with point-of-care blood glucose testing used to confirm clinically important high or low glucose readings and to guide treatment when necessary. The primary outcome is insulin resistance on the first day after surgery, measured using the Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), which is calculated from fasting blood glucose and fasting insulin concentrations. Secondary outcomes include perioperative glucose levels and glucose variability, time spent within, above, and below the target glucose range, insulin and C-peptide levels, postoperative nausea and vomiting, patient comfort, postoperative recovery, hospital stay, postoperative complications, and safety events such as hypoglycemia, severe hyperglycemia, reflux, or aspiration. The main comparison of interest is between the oral carbohydrate group and the standard ERAS group. The intravenous glucose group will be analyzed mainly as a mechanistic exploratory group.

Participants needed: 126
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: The Affiliated Hospital of Qingdao UniversityUpdated: Sep 21, 2026
Eligibility criteria

1.Age 18 to 75 years, regardless of sex. 2.Diagnosis of type 2 diabetes mellitus...

1. Known or highly suspected diabetic gastroparesis, delayed gastric emptying, g...

Status: Recruiting

Functional Capacity and Days Alive Out of Hospital at 30 Days

This prospective observational study aims to compare days alive and out of hospital at 30 days (DAOH-30) in patients with poor or good functional capacity undergoing gastrointestinal surgeries. The investigators are testing the hypothesis that patients with good functional capacity will have longer days alive and out of hospital than those with poor.

Participants needed: 470
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Istanbul UniversityUpdated: May 4, 2025Locations: 1Duration: 90 Days
Eligibility criteria

Patients undergoing intermediate and major upper or lower gastrointestinal surge... [+3]

Day case/ambulatory or one overnight hospital stay for minor gastrointestinal an... [+4]

Status: Recruiting

REmote Symptom COllection to improVE postopeRative Care

There are vulnerabilities in post-discharge care transition for patients after undergoing resection of malignant gastrointestinal tumors. This study aims to investigate the possibility of utilizing Voice-Assisted Remote Symptom Monitoring System (VARSMS) to alleviate some of these challenges.

Participants needed: 281
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Medstar Health Research InstituteUpdated: Apr 3, 2025Locations: 2
Eligibility criteria

At least 18 years old. Ages of subjects >89 will simply be reported as >90. [+3]

Unable to provide informed consent. [+3]

Status: Recruiting

Correlation Analysis of POD and pNCD in Elderly Patients With Gastrointestinal Neoplasms

This is a prospective cohort study to explore the differences of serum indicators between elderly gastrointestinal neoplasms patients with postoperative delirium (POD) who either develop or do not develop long-term postoperative neurocognitive disorders (pNCD).

Participants needed: 165
Trial details
Age: 65-100Biological sex: AllType: ObservationalSponsor: Xuanwu Hospital, BeijingUpdated: Apr 3, 2025Locations: 1Duration: 1 Year
Eligibility criteria

Patients ≥65 years of age who have undergone surgical anesthesia of gastrointest...

Inability to complete cognitive function assessment; Illiteracy, hearing impairm...