Ignite Creation Date:
2024-05-06 @ 8:00 PM
Last Modification Date:
2024-10-26 @ 3:18 PM
Study NCT ID:
NCT06214169
Status:
COMPLETED
Last Update Posted:
2024-01-19
First Post:
2023-12-26
Brief Title:
Effect of Addition of Cisatracurium to Lidocaine VS Plain Lidocaine
Sponsor:
Watim Medical Dental College
Organization:
Watim Medical Dental College
Study Overview
Official Title:
Effect of Addition of Cisatracurium to Lidocaine VS Plain Lidocaine for Intravenous Regional Anesthesia a Comparative Study
Status:
COMPLETED
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this Randomized Control Trial is to compare the effects of addition of cisatracurium to lignocaine for IVRA Vs Plain lignocaine in All ASA physical status I II patients between 20 to 55 years of age scheduled for elective hand surgery carpal tunnel trigger finger tendon release fracture reduction and tendon repair The main questions it aims to answer are Does addition of Cisatracurium to plain lignocaine improve the overall quality of anesthesia Does use of cisatracurium lead to improved postop analgesia and decreased parenteral analgesic requirements Participants will be Forty-four patients undergoing elective hand surgery during IVRA randomly assigned to two groups of 22 patients each All demographic details age gender body weight will be noted all will be briefed about visual analogue score 0 to 10 for pain Group 1 control group will receive lidocaine 2 diluted with saline group 2 cisatracurium group will receive cisatracurium plus lidocaine 2 diluted with saline A standard technique would be employed for IVRA The following parameters to be assessed onset and offset of sensory and motor block Intra-operative pain at 5 10 20 30 minutes after tourniquet application by using visual analogue score VAS and postoperative pain using visual analogue score VAS measured at 5-minute1 2 4 8 hours postoperatively
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None