Remifentanil effect on shoulder surgery postoperative pai
Phase 2
Recruiting
- Conditions
- Shoulder fracture postoperative pain.Dislocation, sprain and strain of joints and ligaments of shoulder girdle
- Registration Number
- IRCT2017050126328N4
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
patients candidate to undergo shoulder surgery; aged between 20 and 60 years old; Class I or II according to ASA classification. Exclusion criteria: history of uncontrollable chronic pain; history of allergy to analgesics; history of psychotropic drugs consumption; recent use of analgesics; operation time more than 2 hours; pregnant and breastfeeding women.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analegsia onset. Timepoint: Postoperative recovery. Method of measurement: Questionnaire.;Patients pain severity after shoulder surgery during recovery. Timepoint: In admission to recovery room and discharge from the recovery. Method of measurement: Using visual analogue scale.
- Secondary Outcome Measures
Name Time Method Administered remifentanil dosage amount. Timepoint: During admission to recovery. Method of measurement: Questionnaire.;Nausea and vomiting due to remifentanil injection. Timepoint: During admission to recovery. Method of measurement: Questionnaire.;Hypotension due to remifentanil injection. Timepoint: During admission to recovery. Method of measurement: Questionnaire.;Bradycardia due to remifentanil injection. Timepoint: During admission to recovery. Method of measurement: Questionnaire.