IRCT20170903036041N1RecruitingPhase 2
Evaluation of Effectiveness of Different Dosage of Neostigmine in Combination with Metoclopramide, on Gastric Residual Volume, in Enteral Nutrition, in Hospitalized Patients in Intensive Care Unit
Vice chancellery for research Iran University of Medical Sciences0 sites165 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Recruiting
- Sponsor
- Enrollment
- 165
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 60 years (—)
- Sex
- All
Inclusion Criteria
- •Enteral nutrition feeding
- •After three hours from the last gavage gastric residual volume =50%
Exclusion Criteria
- •Diabetes mellitus disease
- •Atrioventricular block
- •Heart rate <60
- •Systolic blood pressure <90
- •Within 10 days Gastrointestinal surgery
- •Clinical signs of Gastrointestinal obstruction
- •Bronchospasm or Asthma history
- •In 24 hours administration of Prokinetic drugs
- •Sensitivity to Metoclopramide or Neostigmine
- •Kidney failure or Creatinine >2 milligram/deciliter
- •Hypokalemia
- •Concomitant medication with Cyclosporine
- •Digoxin and Monoamine Oxidase inhibitors
Investigators
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