Duration of post operative pain relief using local anaestheic
Phase 4
- Conditions
- Health Condition 1: M849- Disorder of continuity of bone, unspecifiedHealth Condition 2: S422- Fracture of upper end of humerus
- Registration Number
- CTRI/2019/10/021666
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a)Parents willing to give consent.
b)ASA grade-I,II patients
c)Age: 5-12 years
d) Patients posted for upper and lower limb surgery.
Exclusion Criteria
a)Patients who are allergic to local anaesthetics
b)Patients having coagulopathies.
c)Patients on anticoagulants.
d)Patients with liver failure
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study the duration of post operative analgesia after peripheral nerve block with 0.2% ropivacaine in paediatric patients undergoing upper and lower limb surgeriesTimepoint: 1.Baseline <br/ ><br>2.5min,10min,15min,30min,1hr and then every hour intraoperatively. <br/ ><br>4 10mins.4hr,8hr,12hr,24hr postoperatively <br/ ><br>4. time of rescue analgesia
- Secondary Outcome Measures
Name Time Method To study the duration of sensory block postoperatively after peripheral nerve block with 0.2% ropivacaine in paediatric patients undergoing upper and lower limb surgeries <br/ ><br>2.To study the duration of motor block after peripheral nerve block with 0.2% ropivacaine in paediatric patients undergoing upper and lower limb surgeriesTimepoint: 1.10mins.4hr,8hr,12hr,24hr postoperatively <br/ ><br>