To study difference in time to discharge home following surgery for piles using two different methods of numbing.
Phase 4
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2020/03/024020
- Lead Sponsor
- Gmch
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 44
Inclusion Criteria
1.ASA physical status I and II of either sex.
2.Age between 18 to 65 years.
3.BMI â�¥20 to â�¤ 35 kg m-�².
4.Scheduled for FIA surgery.
Exclusion Criteria
1.Refusal by the patient.
2.Patients with coagulopathy and bleeding disorders.
3.Pre-existing local infection at the site of saddle block.
4.Pregnant or lactating women.
5.Patients having sensory or motor problem in the lower limb.
6.Contraindication or allergy to bupivacaine and diclofenac.
7.Patients having hemodynamic instability.
8.Patients having pain in any other area other than surgery site.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of discharge readiness of patients after surgeryTimepoint: immediately at 0, 5, 10, 15, 30 and 60 minutes after block and also every hourly till 12hours and then 24 hours after the block.
- Secondary Outcome Measures
Name Time Method 1.Modified adtrete score <br/ ><br>2.sensory and motor level <br/ ><br>3.nausea/vomiting <br/ ><br>4.headache/backache <br/ ><br>5.VAS at rest and on movement <br/ ><br>6.rescue analgesic requirement <br/ ><br>7.PR, RR, MAP <br/ ><br>8.Surgeon satisfaction scoreTimepoint: immediately at 0, 5, 10, 15, 30 and 60 minutes and also every hourly till 12hours and then 24 hours after the block.