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Pain and satisfaction score will be assessed at the end of surgery and compared in either of two groups
Full 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
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Inclusion criteria
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Interventional model
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50 participants in 2 patient groups, including a placebo group
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Anum Arif
Data sourced from clinicaltrials.gov
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