Ketamine for pain relief via different routes in children aged 2-6years.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/07/055105
- Lead Sponsor
- Indira Gandhi medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
The study will be carried out in 70 patients in age group of 2years- 6years. ASA I and ASA II after approval by institutional protocol review committee.
Exclusion Criteria
1.Refusal for consent by parents/ guardian.
2.Children with cardiovascular diseases.
3. Any history of bleeding or clotting disorder.
4. Local infection at the site of needle insertion.
5. History of allergy to local anaesthetics of ketamine.
6. Children with coagulopathy, pilonidal sinus or local site infections.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare duration of prospective pain free period in paediatric patients following administration of subanaesthetic doses of intravenous ketamibe plus caudal bupivacaine to caudal bupivacaine plus ketamineTimepoint: 24hrs
- Secondary Outcome Measures
Name Time Method Secondary outcome in form of postoperative agitation, sedation etc.Timepoint: 24hrs;To evaluate requirement of rescue analgesia postoperativelyTimepoint: 24hrs;To measure the duration of pain free period & amount of analgesic consumption in first 24hrs postoperativelyTimepoint: 24hrs