Comparación de los efectos de Apotel y Ketorolac antes de la cirugía sobre el dolor y la cantidad de narcóticos necesarios después de la cirugía abdominal

Phase 3

• Conditions: Pain after abdominal surgery.; Unspecified complication of procedure; T81.9

• Registration Number: IRCT20230911059408N1
• Lead Sponsor: Islamic Azad University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 128

Inclusion Criteria

Elective surgery
ASA1,2 (American Society of Anesthesiologists)
Age 18-65 years
Signing a personal consent form to enter the study
No abuse of drugs, alcohol, cigarettes and psychotropic drugs

Exclusion Criteria

Loss of consciousness
Hemodynamic disorder
Abnormal intraoperative bleeding
The length of the operation more than 4 hours

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: 1, 6, 12, 24 hours after the operation. Method of measurement: Visual Analogue Scale.