Evaluation of the effect of ketamine-metoclopramide and acetaminophen-metoclopramide on pain intensity after deep vitrectomy operatio
Phase 3
Recruiting
- Conditions
- Deep vitrectomy operation.Other specified postprocedural statesZ98.89
- Registration Number
- IRCT20200825048515N4
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 96
Inclusion Criteria
Candidates for vitrectomy operation under general anesthesia
Hospitalization of patients after surgery for at least 24 hours
Patients ability to communicate with clinicians
Patients with anesthesia criteria with ASA I and ASA II
surgery duration less than 3 hours and more than 1 hour
Exclusion Criteria
Patients with pain syndromes
Patients with a history of drug and drug addiction
Any uncontrolled systemic disease
Psychological and neurological diseases
Any allergies to the studied drugs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: Upon entering the recovery, 15 minutes and 30 minutes later,Exit-recovery, then at 4, 8, 16 and 24 hours after surgery. Method of measurement: VAS scoring system.;Nausea. Timepoint: Upon entering the recovery, 15 minutes and 30 minutes later,Exit-recovery, then at 4, 8, 16 and 24 hours after surgery. Method of measurement: VAS scoring system.;Time to extubation. Timepoint: From the time of discontinuation of the anesthetic to the exit of the endotracheal tube. Method of measurement: Patient file.
- Secondary Outcome Measures
Name Time Method