A study to compare effects of different combinations of drugs when given in caudal block for surgery involving below umblicus.
Not Applicable
- Conditions
- Health Condition 1: null- any child undergoing lower abdominal surgery for any disease
- Registration Number
- CTRI/2018/09/015673
- Lead Sponsor
- Jyoti
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 66
Inclusion Criteria
children in ASA status 1 and 2 undergoing any type of surgical procedure in the lower abdominal region
Exclusion Criteria
ASA status 3,4 or 5
Any contraindication to caudal block such as scaral agenesis, tumors, local infection
history of seizures
hypersensitivity to any of the drugs in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method time duration of analgesia in the post operative periodTimepoint: time duration of analgesia in the post operative period measured at 5, 10, 15,30,45,60,90 minutes
- Secondary Outcome Measures
Name Time Method hemodynamic stability in the intra operative periodTimepoint: 5,10,15,30,45,60,90 intra operatively