A comparative study of Fentanyl and Clonidine to assess analgesia in pediatric patients undergoing lower abdomen surgeries.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: N288- Other specified disorders of kidney and ureter
- Registration Number
- CTRI/2024/04/065745
- Lead Sponsor
- Dr Vaidehi Chavan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA physical status 1 and 2,
2. Elective infra-umbilical and genitourinary surgeries
Exclusion Criteria
1. Parent unwillingness
2. Infection at block site
3. Bleeding diathesis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesia in the postoperative period.Timepoint: 0 hr, 1 hr, 2 hr, 3 hr, 4 hr, 6 hr, 8 hr, 10 hr, 12 hr.
- Secondary Outcome Measures
Name Time Method To compare the duration of post operative analgesia provided by each group and associated side effects.Timepoint: 0 hr, 1 hr, 2 hr, 3 hr, 4 hr, 6 hr, 8 hr, 10 hr, 12 hr.