A study for postoperative pain relief using two drugs in combination in patients undergoing arthroscopic shoulder surgery.
Not Applicable
- Conditions
- Health Condition 1: null- Patients fit for shoulder surgeries
- Registration Number
- CTRI/2018/05/013671
- Lead Sponsor
- Department of Anaesthesia and Intensive Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anesthesiologists (ASA)
physical status I-II
BMI â?? 18-30 kg/m2
Undergoing Arthroscopic shoulder surgery such
as rotator cuff injury repair, recurrent
shoulder dislocations, superior labrum
anterior and posterior (SLAP lesion),
acromioplasty, labral cyst removal.
Exclusion Criteria
Patient refusing to give informed consent
History of relevant drug allergy
History of psychiatric illness, substance
abuse
Severe cardiovascular, respiratory, metabolic
or neurological disease
Pregnancy and lactation
Coagulopathy
Contralateral phrenic nerve dysfunction
Infection at planned injection site
Patients on steroids
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean postoperative pain score measured by numeric rating scale(NRS) over 48h study period.Timepoint: Mean NRS pain score between the two groups over 48h study period at time intervals of 1,4,12,24,36,48h.
- Secondary Outcome Measures
Name Time Method Difference in total analgesic consumption, rescue analgesic use, manual muscle test scoring, patient satisfaction and adverse effects if any. <br/ ><br>Timepoint: Difference in total analgesic consumption, rescue analgesic use, manual muscle test scoring, patient satisfaction and adverse effects if any checked at intervals of 1,4,12,24,36,48 hour time period. <br/ ><br>