Comparison of the effects of Ketamine-Metoclopramide and Acetaminophen-Metoclopramide in deep Vitrectomy surgery
Phase 3
- Conditions
- Vitrectomy.Disorders of vitreous body
- Registration Number
- IRCT20150106020588N9
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
Candidate for Vitrectomy surgery
Age 40 to 80 years
ASA class I and II
Informed consent to enter the study
Exclusion Criteria
History for abusing the drugs, alcohol and psychedelics
Known allergy to ketamine, Acetaminophen, and Metoclopramide
History of mental illness and seizures
Pregnancy and breastfeeding
Body Mass Index (BMI) greater than 35
Taking painkillers 24 hours before surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of pain after the operation. Timepoint: Upon entering recovery, 30 minutes, 2 hours, 4 hours, 8 hours, 24 hours after surgery. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Heart Rate. Timepoint: Upon entering recovery, 30 minutes, 2 hours, 4 hours, 8 hours, 24 hours after surgery. Method of measurement: Electrocardiogram.;Blood Pressure. Timepoint: Upon entering recovery, 30 minutes, 2 hours, 4 hours, 8 hours, 24 hours after surgery. Method of measurement: Sphygmomanometer.