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Effect of prophylactic 2 g paracetamol in reducing of postoperative pain after gynecologic laparoscopy

Not Applicable
Conditions
Acute postoperative pain.
Acute pain
Registration Number
IRCT201312147013N5
Lead Sponsor
Vice chancellor for research, Tabriz University of Medical? Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
92
Inclusion Criteria

ASA class I, II; scheduled for gynecologic laparoscopy; age 20-70 years. Exclusion criteria: laparatomy with laparoscopy; allergy to paracetamol; history of organ system dysfunction( cardiovascular, respiratory, liver, renal, ...); history of psychopathy; history of chronic pain syndrome; pregnancy.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: PACU and at 1, 2, 3, 6, 12, and 24h postoperatively. Method of measurement: visual analogue scale (0= non to 10= severe pain) cm).
Secondary Outcome Measures
NameTimeMethod
Postoperative analgesic consumption. Timepoint: PACU and during 24h postoperatively. Method of measurement: number and amount of medication by mg.
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