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Gastrointestinal Hemorrhage clinical trials

View clinical trials related to Gastrointestinal Hemorrhage.

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NCT ID: NCT00190255 Completed - Clinical trials for Gastrointestinal Hemorrhage

Pharmacogenetics of Gastrointestinal Bleeding

Start date: April 2004
Phase: Phase 4
Study type: Observational

Gastrointestinal bleeding is a severe adverse effect occurring in subjects secondary to the use of nonsteroidal anti-inflammatory drugs (NSAIDs). The enzyme CYP2C9 is responsible for the elimination of several NSAIDs. This protein is inactive in 12% of the subjects because of genetic mutations. We hypothesized that individuals carrying such mutations should be at higher risk of gastrointestinal bleeding since they display decreased NSAIDs elimination.

NCT ID: NCT00164866 Completed - Peptic Ulcer Clinical Trials

Administration of High-Dose Intravenous Proton Pump Inhibitor for Upper Gastrointestinal Bleeding Prior to Endoscopy

Start date: February 2004
Phase: Phase 4
Study type: Interventional

To evaluate if intravenous PPI infusion, when administered prior to endoscopy, hastens resolution of bleeding stigmata and thereby facilitates endoscopic examinations and reduces the need for endoscopic treatment. Clot stabilization may itself sustain control of bleeding before endoscopy. These may translate into improved patients’outcome and survival. To determine the therapeutic effect of high-dose PPI infusion in upper gastrointestinal bleeding from causes other than peptic ulcers.

NCT ID: NCT00164788 Terminated - Clinical trials for Gastrointestinal Hemorrhage

A Comparison of Gastric pH Control With High Dose Intravenous or Oral Esomeprazole

Start date: July 2004
Phase: Phase 2
Study type: Interventional

The investigators hypothesize that high dose esomeprazole 80mg given as a bolus, followed by 8mg/h would render gastric pH near neutral and that pH control with esomeprazole given in such a high dose either intravenous or orally is identical.

NCT ID: NCT00164723 Completed - Clinical trials for Gastrointestinal Hemorrhage

Endoscopic Evaluation of Lower Gastrointestinal Bleeding (GIB) in Patients Presenting With Melena

Start date: February 2005
Phase: N/A
Study type: Interventional

To evaluate the incidence and etiology of small bowel or large bowel bleeding in patients presenting with melena.

NCT ID: NCT00153686 Completed - Clinical trials for Gastrointestinal Hemorrhage

Capsule Endoscopy or Mesenteric Angiogram in Patients With Overt Gastrointestinal Bleeding (GIB) of Obscure Origin

Start date: June 2005
Phase: N/A
Study type: Interventional

To compare the diagnostic yield of mesenteric angiogram with CE in patients with active obscure GIB.

NCT ID: NCT00152399 Completed - Peptic Ulcer Clinical Trials

Study to Assess the Efficacy and Safety of Somatostatin in the Treatment of Acute Severe Upper Gastrointestinal Bleeding

Start date: September 2000
Phase: Phase 2
Study type: Interventional

To assess the efficacy and safety of the early administration of somatostatin in infusion during 72 hours plus 2 boluses, compared to placebo in the control of acute severe UGIB with suspicion of PUB.

NCT ID: NCT00045799 Completed - Clinical trials for Upper Gastrointestinal Bleeding

Safety & Efficacy of Omeprazole Sodium Bicarbonate for the Prevention of Upper GI Bleeding in the Critically Ill

Start date: May 2002
Phase: Phase 3
Study type: Interventional

Critically ill patients are at an increased risk of having upper gastrointestinal (GI) bleeding due to stress related mucosal damage. Cimetidine, delivered continuously through intravenous infusion, is the only drug that the FDA has approved for the prevention of upper GI bleeding in critically ill patients. The present trial is intended to assess the safety and efficacy of an omeprazole sodium bicarbonate immediate-release suspension in this indication.

NCT ID: NCT00004327 Completed - Clinical trials for Hereditary Hemorrhagic Telangiectasia

Phase II Pilot Study of Octreotide, a Somatostatin Octapeptide Analog, for Gastrointestinal Hemorrhage in Hormone-Refractory Hereditary Hemorrhagic Telangiectasia and Senile Ectasia

Start date: January 1995
Phase: Phase 2
Study type: Interventional

OBJECTIVES: I. Evaluate the efficacy of octreotide, a somatostatin octapeptide analog, in decreasing gastrointestinal bleeding in patients with hormone-refractory hereditary hemorrhagic telangiectasia or senile ectasia.