To study the effect of clonidine when added to bupivacaine for spinal anesthesia in pediatric patients posted for below umbalical surgery.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/02/017782
- Lead Sponsor
- Amol Bhalerao
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Age group between 1 to 10 yr.
2) Either sex
3) Pediatric patients sheduled for lower abdominal, urological and lower limb surgery.
4) ASA status 1 and 2
Exclusion Criteria
1) Contraindications for spinal anesthesia.
2) Lower respiratory tract infection.
3) Allergy to bupivacaine or clonidine.
4) Parental refusal.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Study the duration of surgical anesthesia and duration of post operative analgesia.Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Study the effect of intrathecal clonidine on hemodynamic parameters, sedation and look for any adverse effect.Timepoint: Till 24 hr