Non-variceal Upper Gastrointestinal Bleeding

2

Review clinical trials related to Non-variceal Upper Gastrointestinal Bleeding. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Keverprazan vs Pantoprazole for the Treatment of ANVUGIB

Acute non-variceal upper gastrointestinal bleeding (ANVUGIB) is a common medical emergency requiring hospitalization. The cornerstone of ANVUGIB management is effective gastric acid suppression. Potassium-competitive acid blockers (P-CABs) represent a novel class of gastric acid secretion inhibitors, which can rapidly and consistently increase intragastric pH. Keverprazan, a novel P-CAB, has been shown to be effective in treating duodenal ulcers and erosive esophagitis. Herein, we have designed a multicenter randomized controlled trial (RCT) to determine whether keverprazan is noninferior to pantoprazole in preventing rebleeding after successful initial hemostasis in patients with ANVUGIB.

Participants needed: 908
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: General Hospital of Shenyang Military RegionUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Participants presented with hematemesis, melena, or other clinical manifestation... [+3]

Participants have experienced failure of endoscopic hemostasis, rebleeding befor... [+10]

Status: Recruiting

The Difference in Carbon Footprint Between Diagnostic Upper GI Endoscopy in Dyspeptic Patients Versus Therapeutic Upper GI Bleeding

The goal of this observational study is to learn about the carbon footprint produced from diagnostic upper GI endoscopy in patients with dyspepsia and therapeutic upper GI endoscopy in patients with non-variceal upper GI bleeding. The main question it aims to answer is: • How much carbon footprint is generated from upper GI endoscopy Participants are already receiving diagnostic and therapeutic upper GI endoscopy as part of their regular medical care for dyspepsia and non-variceal upper GI bleeding, respectively. The carbon footprint generated from this treatment process is examined.

Participants needed: 75
Trial details
Age: 20-80Biological sex: AllType: ObservationalSponsor: King Chulalongkorn Memorial HospitalUpdated: Dec 3, 2025Locations: 2
Eligibility criteria

Patients with dyspepsia or non-variceal upper GI bleeding [+2]

Platelet < 50,000 [+5]