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Endoscopic Application of Tranexamic Acid and Sucralfate in Gastrointestinal Tumor Bleeding: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Background Gastrointestinal bleeding is a common disease among the population in Taiwan, with gastrointestinal tumor bleeding accounting for 3-5% of cases. The pathophysiology of gastrointestinal tumor bleeding is unique, involving fragile surface mucosa, abnormal vascular proliferation, and malformation, making endoscopic hemostasis challenging. Conventional endoscopic hemostasis methods such as hemostatic injections, clips, or thermal coagulation have suboptimal success rates below 80%, with recurrence rates exceeding 50%. Recent clinical trials have demonstrated that hemostatic powder spraying effectively enhances hemostasis for gastrointestinal ulcers and reduces recurrence rates. Our previous research repurposed tranexamic acid in a powder form to enhance hemostasis for peptic ulcer and applied sucralfate powder to prevent postpolypectomy wound bleeding. Study aim Our research team combines previous experience by using tranexamic acid and sucralfate drug powders to spray onto bleeding gastrointestinal tumors to achieve hemostatic effects. Additionally, tumor-derived exosomes are associated with tumor angiogenesis and growth, so we hypothesize that gastrointestinal tumor bleeding may be linked to VEGF and miR-21 expression within gastrointestinal tumor exosomes. Study method This study is a clinical randomized controlled trial conducted at National Cheng Kung University Hospital. We will recruit 60 patients with gastrointestinal tumor bleeding undergoing endoscopic hemostasis. Patients in the experimental treatment group will receive additional topical administration of 1.5 g of tranexamic acid and 3 g of sucralfate drug powder. Immediate hemostasis and 30-day bleeding recurrence will be observed. Enrolled patients will also provide blood and tumor specimens for exosome analysis, evaluating the predictive effect of extracted tumor exosomes' VEGF and miR-21 on bleeding risk. This study will explore the association between specific tumor exosome expression levels and bleeding, serving as a basis for bleeding risk assessment and innovative therapies.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• patients aged ≥ 18 years who accept endoscopy for upper GI tumor bleeding

Locations
Other Locations
Taiwan
National Cheng Kung University Hospital
RECRUITING
Tainan
Contact Information
Primary
Hsueh-Chien Chiang, MD
scion456scion@gmail.com
8862353535
Time Frame
Start Date: 2026-05-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 60
Treatments
Experimental: intervention group
For patients in both the standard group and intervention group, epinephrine injection, clipping, and heat coagulation will be applied. The decision for the choice of standard therapy was left to the discretion of the endoscopist in the absence of any recommendations or proof of superiority of one modality over another in the initial endoscopic approach to use in patients presenting with malignant bleeding. For patients in the intervention group, we will additionally deliver 3g of sucralfate powder and 1.5g of tranexamic acid powder through the endoscopy precisely on the bleeding site after conventional therapy.
Active_comparator: Standard group
For patients in both the standard group and intervention group, epinephrine injection, clipping, and heat coagulation will be applied. The decision for the choice of standard therapy was left to the discretion of the endoscopist in the absence of any recommendations or proof of superiority of one modality over another in the initial endoscopic approach to use in patients presenting with malignant bleeding.
Related Therapeutic Areas
Sponsors
Leads: National Cheng-Kung University Hospital

This content was sourced from clinicaltrials.gov

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