comparision between the effects of plain chloroprocaine and chloroprocaine with fentanyl in spinal anaesthesia

Not Applicable

Completed

• Conditions: Health Condition 1: N398- Other specified disorders of urinary system

• Registration Number: CTRI/2018/12/016687
• Lead Sponsor: Sri Ramachandra Institute of Higher Education and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-10-31
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 106

Inclusion Criteria

Patients undergoing endoscopic urologic surgeries

ASA-I,II

Exclusion Criteria

Patient refusal

Allergy to local anaesthetics

Patient on anticoagulants or bleeding disorders

Infection at site of injection

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Onset of sensory blockade <br/ ><br>Maximum height of block achieved <br/ ><br>Onset time for complete motor blockade <br/ ><br>Regresssion time to L1 and return of bromage score to 0 <br/ ><br>Timepoint: sensory level will be assessed after three minutes of drug injection. Thereafter, sensory level is checked for every , <br/ ><br>3min until 15min, every 5min until the end of surgery and then for every 10min for 60min and every 15min until block regresses to L1. <br/ ><br> Using Bromage scale Motor block is assessed <br/ ><br>For every 3min for 15min <br/ ><br>At the beginning and at the end of the surgery <br/ ><br>After the surgery for every 10min for 60min, then every 15minutes until the block regress to S2.

Secondary Outcome Measures

Name	Time	Method
Any head tilt <br/ ><br>Time to first postoperative analgesia <br/ ><br>Any adverse eventsTimepoint: Vitals(BP,HR,RR,SPO2)noted for every 5min interval from the starting of surgery to end of surgery and then every 15min until block regressess to L1.