Study to see the effect of analgesia in post operative pain in perianal surgery.
Not Applicable
- Conditions
- Health Condition 1: L988- Other specified disorders of the skin and subcutaneous tissue
- Registration Number
- CTRI/2024/08/072126
- Lead Sponsor
- Dr Shruti Priya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Posted for electric peri-anal surgeries like fistula-in-ano, fissure, pilonidal sinus.
2. Surgery under spinal anaesthesia.
Exclusion Criteria
1. Patient refusal.
2. Allergy to study drugs.
3. Pregnancy.
4. Acute peri-anal abscess and anorectal cancer.
5. Failed spinal block.
6. Inability to understand patient information leaflet and NRS score
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare time of first analgesia requirement in minutes when NRS greater than 4Timepoint: In postoperative at interval of just after surgery-1hr-2hr-4hr-8hr.
- Secondary Outcome Measures
Name Time Method 1. To compare total dose of analgesic requirement in term of morphine equivalent <br/ ><br>2. To compare patient satisfaction score after surgery. <br/ ><br>3. To compare the incidence of side effectTimepoint: 1. In 1st 24hrs postoperative. <br/ ><br>2. In 1st 24hrs postoperative. <br/ ><br>3. In 1st 24hrs postoperative.