Ondansetron femoral nerve block

Not Applicable

• Conditions: Surgery; postoperative analgesia

• Registration Number: PACTR201608001746591
• Lead Sponsor: Tanta University, Faculty of Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-08-20
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

age 18 ¿ 40 years
either gender
ASA I-II
undergoing elective arthroscopic anterior cruciate ligament reconstruction (ACLR)

Exclusion Criteria

body mass index > 35
mental disorders
any contraindication to regional anesthesia (e.g. local infection, coagulation abnormality, or patient refusal)
known allergy to the study drug
pregnancy
drug or alcohol abuse
a daily intake of opioid analgesics

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
visual analogue score of pain VAS

Secondary Outcome Measures

Name	Time	Method
¿Time of first analgesic request;¿Total consumption of rescue analgesia ;¿Postoperative mean arterial blood pressure, heart rate ;¿Any concomitant events like nausea; vomiting, shivering, pruritus or respiratory complications ;¿The overall patient satisfaction