Gastrointestinal Hemorrhage
Conditions
Keywords
Hemostasis, Endoscopic; Randomized Controlled Trial
Brief summary
Bipolar hemostatic forceps will be tested against standard therapy in active, non-variceal, upper gastrointestinal bleeding by a prospective, randomized trial
Detailed description
Patients with active, non-variceal, upper gastrointestinal bleeding usually need an urgent endoscopic treatment. The standard therapy by application of an hemoclip and/or injection of an epinephrine solution is not always successful. Bipolar hemostatic forceps is already being used successfully for the treatment of gastrointestinal bleeding in endoscopic submucosal dissection. Its use in primary endoscopic treatment of non-variceal, upper gastrointestinal bleeding has not been shown yet in a randomized prospective study. Patients with active, non-variceal, upper gastrointestinal bleeding (esophagus or stomach or duodenum) of any cause are randomized (1:1) in standard therapy by combination therapy using an hemoclip and/or injection of an epinephrine solution or experimental therapy by application of the bipolar hemostatic forceps. Cross over-treatment should be tried first in case of failed initial treatment. Rescue treatment by other methods such as application of an Over the Scope Clip (OTSC), angiographic embolization or surgery will be allowed next. All patients receive an additional standard therapy by proton pump inhibitors (PPI). Hypothesis: Endoscopic therapy by application of the bipolar hemostatic forceps is superior to standard therapy regarding technical success and rebleeding rate.
Interventions
Bipolar hemostatic forceps
Endoscopic therapy with hemoclip +/- injection of epinephrine solution
Sponsors
Study design
Intervention model description
Randomized prospective study
Eligibility
Inclusion criteria
* Active, nonvariceal, upper gastrointestinal bleeding
Exclusion criteria
* Severe coagulopathy unresponsive to blood products transfusions: platelets \<20,000; international normalized ratio \>3.0; partial thromboplastin time \>2 normal
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Successful primary hemostasis | 15 minutes | Number of participants without further endoscopically visible gastrointestinal bleeding in esophagogastroduodonoscopy |
| Rebleeding | 30 days | Number of participants without recurrent endoscopically visible gastrointestinal bleeding in esophagogastroduodonoscopy |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Reinterventions | 30 days | Number of endoscopic reinterventions for gastrointestinal bleeding |
Countries
Germany