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Clinical Trial Summary

Pain and satisfaction score will be assessed at the end of surgery and compared in either of two groups


Clinical Trial Description

All patients meeting inclusion criteria will be randomly enrolled in two groups. Intervention group will receive buffered lignocaine . at the end of procedure data will be recorded regarding pain VASscore and satisfaction score ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04610307
Study type Interventional
Source Combined Military Hospital, Pakistan
Contact Anum Arif
Phone +923422398424
Email dranumarif@yahoo.com
Status Not yet recruiting
Phase N/A
Start date November 1, 2020
Completion date December 1, 2020

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