Comparing the two methods of analgesia for assessing pain relief after surgery in children undergoing Hip/thigh surgeries.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/04/051707
- Lead Sponsor
- Sherlina Dolly E
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1, ASA 2, Stable ASA 3 children
Exclusion Criteria
Age >18 years
Uncontrolled systemic illness such as diabetes mellitus ,cardiac ailment
Infection at the injection site
Bleeding diasthesis
Not willing to participate in the trial
Allergic to local anaesthetics.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of hypotension between the two groupsTimepoint: Immediate post op <br/ ><br>6 hrs post op <br/ ><br>Day 1 <br/ ><br>Day 2 <br/ ><br>Day 3
- Secondary Outcome Measures
Name Time Method Post operative analgesia using FLACC and CHEOPS Score <br/ ><br>vascular injury <br/ ><br>Nerve injury <br/ ><br>Urinary retention <br/ ><br>motor blockade <br/ ><br>Time of initiation of first dose,frequency and total doses of NSAIDS and opiods postoperatively administered. <br/ ><br>Timerequired for initiation of ambulation and length of hospital stay. <br/ ><br>Adverse effects if anyTimepoint: Immediate post op <br/ ><br>6 hrs post op <br/ ><br>Day 1 <br/ ><br>Day 2 <br/ ><br>Day 3