Effect of a drug on pain management given with regional block to reduce pain after surgery
Not Applicable
- Conditions
- Health Condition 1: S599- Unspecified injury of elbow and forearm
- Registration Number
- CTRI/2020/05/025021
- Lead Sponsor
- Dr Ankita Rawat
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients with ASA grade I and II.
2.Age group 18- 60 years
3 Patient undergoing upper limb surgery under axillary block
Exclusion Criteria
1.Patient refusal
2.ASA grade III & IV patients
3.History of allergy or sensitivity to local anaesthetic or study drug
4. Known cardiovascular respiratory disease
5.Known hepato renal disease
6.Neuropsychiatric disorders
7.History of bleeding disorder..
8.Day care surgery
9.Pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate for the duration of post-operative analgesiaTimepoint: To evaluate for the duration of post-operative analgesia
- Secondary Outcome Measures
Name Time Method 1 .To evaluate the onset of sensory and motor block <br/ ><br>2 To compare the complete effect of sensory and motor block <br/ ><br>3. To assess for patient satisfaction <br/ ><br>4. To evaluate the adverse effects like nausea, vomiting, dysarrhythmias, hypotension, <br/ ><br> bradycardia, convulsions, sedation, neurological problems and hypersensitivity reaction for the study drug . <br/ ><br> <br/ ><br>Timepoint: 1.from administration of drug upto the 30 minutes of surgery for sensory and motor block assessment <br/ ><br> <br/ ><br>2.Visual analogue scoring for oain from the point completion of surgery upto 24 hrs