Continuous wound infusio

Not Applicable

Recruiting

• Conditions: Surgery; acute post-operative pain

• Registration Number: PACTR201507000961407
• Lead Sponsor: Faculty of Medicine. Tanta University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-12-06
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

ASA class I and II
age 18-60
either gender
scheduled for open inguinal hernia repair

Exclusion Criteria

history of cardiac disease
impaired renal or hepatic function
coagulation disorders
hypertensive patients treated with ¿-methyldopa, clonidine or ¿-adrenergic blockers
using opioid or non-opioid analgesics within the previous 72 h
contraindication to the study drugs.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
visual analogue pain scale (VAS);rescue analgesia: pethidine consumption

Secondary Outcome Measures

Name	Time	Method
mean aterial blood pressure(MAP) , heart rate (HR);adverse effects: nausea, vomiting, sedation, local anesthetic toxicity, local inflammation or infection