A clinical trial to compare 1% Chloroprocaine (short acting local anesthetic) inSpinal anesthesia with or without Fentanyl for Enhanced Recovery after Perianal Surgeries
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/02/031417
- Lead Sponsor
- Government medical college Patiala
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of 20 -80 years of age with perianal disease
Exclusion Criteria
1 Patientâ??s refusal
2 Any abnormality of spine
3 Any skin infection or local cellulitis.
4 Any coagulation defect.
5 Recent myocardial infarction or heart disease
6 Patients on anticoagulant drugs
7 Patients with neurological disorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset of sensory and motor block <br/ ><br>Intraoperative hemodynamics <br/ ><br>Maximum sensory block <br/ ><br>Time taken to achieve maximum sensory block and for 2 segment regression of sensory blockade <br/ ><br>Time for rescue analgesia <br/ ><br>Duration of analgesia <br/ ><br>Duration of motor block <br/ ><br>Time to unassisted ambulation <br/ ><br>Time to unassisted voiding <br/ ><br>Timepoint: Sensory blockade will be assessed by loss of pinprick sensation to 23 G hypodermic needle every 2 min for 10 min until highest level is achieved then every 5 min until 2 segment regression. <br/ ><br>Motor blockade will be assessed by Modified Bromage score every 5 min till complete motor block is achieved. <br/ ><br>Intraoperative vitals will be checked every 2 min for 10 min then every 10 min till completion of surgery. <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method ComplicationsTimepoint: Intraoperatively and within 24 hours to 7 days after surgery