Effect of GLP-1 on Intestinal Barrier Function in SBS-IF Patients: A Preliminary Exploration. (NCT07297238) | Clinical Trial Compass
RecruitingNot Applicable
Effect of GLP-1 on Intestinal Barrier Function in SBS-IF Patients: A Preliminary Exploration.
China20 participantsStarted 2026-01-24
Plain-language summary
Eligible patients were randomized into two groups: the GLP-1 group and the control group. The control group received a placebo along with standard care, without any additional GLP-1-based intervention. The GLP-1 group, in addition to standard care, received a subcutaneous injection of a GLP-1 analog (semaglutide injection) strictly according to the drug manufacturer's instructions. The initial dose of semaglutide was 0.25 mg once weekly. Treatment was continued over a 28-days period. Primary and secondary outcomes will be collected.
Who can participate
Age range18 Years – 80 Years
SexALL
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Inclusion Criteria:
* Participants voluntarily provided written informed consent for this trial;
* Aged 18 to 80 years, inclusive, regardless of gender;
* With stable vital signs;
* Diagnosis of SBS-IF, confirmed by existing medical/surgical records, receiving parenteral nutrition (PN) due to surgical resection of the small intestine (\<200 cm from the duodenojejunal flexure), and meeting one of the following criteria:
* Colon continuity maintained without jejunal/ileal stoma (Type II or III);
* Presence of a jejunostomy or ileostomy (Type I);
* Expected requirement of PN for more than 4 weeks, with an average PN caloric intake ≥80%;
* Ability to comply with the medication dosing and visit schedule;
* Capacity to accurately describe symptoms, absence of severe infections or respiratory insufficiency, and willingness to cooperate proactively;
* No history of allergic diseases, non-allergic constitution, and no hypersensitivity to any component of semaglutide injection;
* No history of drug abuse;
* Not pregnant or lactating; no pregnancy plans within one month after the trial (applies to both female and male participants);
* No participation in any other drug trials (including the investigational product in this study) within three months prior to enrollment.
Exclusion Criteria:
* Individuals who do not meet the inclusion criteria or are deemed ineligible by the investigator;
* Poor general condition, inability to accurately describe symptoms, presence of severe inf…
What they're measuring
1
Serum Biomarkers of Intestinal Barrier Function
Timeframe: the initiation of enrollment and upon completion of the 28-days treatment period