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Effects of Enteral Nutrition on Stress Ulcer Hemorrage. Multicenter Randomized Controlled Trial

T

TC Erciyes University

Status

Unknown

Conditions

Gastro Intestinal Bleeding
Proton Pump Inhibitor
Enteral Nutrition
Stress Ulcer Prophylaxis

Treatments

Drug: enteral nutrition + proton pump inhibitor
Other: enteral nutrition only

Study type

Interventional

Funder types

Other

Identifiers

NCT03098537
2016/427

Details and patient eligibility

About

Enteral nutrition can provides prophylaxis against stress ulcer bleeding in critically ill patients and there may be no need to use acid suppressing drugs for stress ulcer bleeding prophylaxis in these patients. Half of the patients on enteral nutrition will not receive any acid suppressing drugs while other half receives it. They will be followed for gastrointestinal bleeding.

Full description

Mucosal erosions can occur on luminal surface of stomach in approximately 75-100% patients during the first 24 hours of intensive care unit admission. These erosions often cause bleeding with penetrating superficial capillaries. Clinically significant bleeding (Significant decrease in blood pressure or decrease in hemoglobin level of more than 2 g / dL) appears to be less than 5% in ICU patients.

Enteral nutrition (EN) has protective effects against stress ulcer bleeding by neutralizing the acidic pH in the stomach lumen, providing a structural and functional integrity of the mucosal surface and trophic effect on the GI mucosa. These effects have been shown in some studies. The above-mentioned studies are inadequate for clinicians to make suggestions for relation between enteral nutrition and stress ulcer hemorrhage.

The risk factors for stress ulcer hemorrhage are mechanical ventilation, coagulopathy and burns.

Proton pump inhibitors (PPI) and histamine receptor blockers (H2RB) are the main drugs used for stress ulcer bleeding prophylaxis.

Studies have shown that 90% of patients admitted to intensive care units receive prophylaxis for stress ulcer bleeding.

Drugs (H2RB, PPI) used for prophylaxis against stress ulcer bleeding have some undesirable harmful effects in critical illnesses. These drugs, which suppress gastric acid secretion, can cause hospital-associated pneumonia and Clostridium difficile enterocolitis.

The studies, for clinical proposals are generally performed in the 1980s and early 1990s. Oral intake was stopped in most of the critically ill patients and early enteral nutrition was not widely used at the time of these major studies performed. Patients who are receiving EN have been shown to develop less stress ulcer bleeding in some studies. In a limited number of animal studies, enteral feeding has been shown to protect stress-related mucosal damage in the gastric mucosa.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 years or older
  • Admission to ICU
  • Expected to stay in ICU >24 hours
  • No contraindications to EN within the first 24 hours after admission to the intensive care unit

Exclusion criteria

  • Evidence of active GI bleeding during current hospitalization prior to study entry
  • Coagulopathy (PLT<50.000, INR>1.5, aPTT>2xcontrol)
  • Patients receiving acid suppressing drugs prior to admission
  • Pregnancy or lactation
  • History/documented gastric ulcer
  • Burn>30% body surface area
  • Head injury or increased intracranial pressure
  • Partial or complete gastrectomy
  • Shock
  • Multi-system trauma
  • Exposure to gastric irritant drugs
  • Patients not giving informed consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

500 participants in 2 patient groups

Enteral nutrion only
Active Comparator group
Treatment:
Other: enteral nutrition only
Enteral nutrion + proton pump inhibitor
Other group
Treatment:
Drug: enteral nutrition + proton pump inhibitor

Trial contacts and locations

1

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Central trial contact

Murat Sungur, MD; Kurat Gundogan, MD

Data sourced from clinicaltrials.gov

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