A study comparing duration of postoperative analgesia after shoulder block in patients undergoing shoulder arthroscopy.
Not Applicable
- Conditions
- Health Condition 1: M258- Other specified joint disorders
- Registration Number
- CTRI/2020/11/029253
- Lead Sponsor
- Vardhman Mahavir Medical College and Safdarjung hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1-2, scheduled for elective unilateral arthroscopic shoulder surgery.
Exclusion Criteria
1) history of allergy to local anaesthetic
2) contraindication to block
3) previous neurological deficit in upper limb
4) BMI >30 KG/m2
5) inability to understand pain scale (VAS)
6) pulmonary, renal, cardiac, hepatic disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the efficacy and duration of post-op analgesia provided by intravenous dexmedetomidine after shoulder block using VAS.Timepoint: 0,2,4,6,12,24 hours
- Secondary Outcome Measures
Name Time Method To compare patient satisfaction in form of quality of pain relief using LIKERT SCALETimepoint: 24 hrs;To compare total amount of rescue analgesia required in each group over 24 hours.Timepoint: 0,2,4,6,12,24