eostigmine-lidocaine admixture for tourniquet pain management in Bier's block

Not Applicable

• Conditions: Injury, Occupational Diseases, Poisoning; Surgery; upper limb surgeries; Anaesthesia

• Registration Number: PACTR201801002886341
• Lead Sponsor: Cairo university hospitals

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-12-17
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 62

Inclusion Criteria

Patients submitted to elective forearm and hand surgeries.
Age between 18-65 years.
Males and females.
ASA physical status I and II.

Exclusion Criteria

¿ Patients suffering from any of the subsequent medical problems:bronchial asthma, Raynaud¿s disease, Sickle cell anaemia, cardiac conduction abnormalities.
¿ Allergy to either lidocaine and/or neostigmine.
¿ Emergency surgeries.
¿ Surgeries exceeding 1 hour duration.
¿ Patients subjected to general anesthesia during surgery.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
intraoperative fentanyl consumption for each group.

Secondary Outcome Measures

Name	Time	Method
Onset of tourniquet Pain.;Number of patients suffering from tourniquet pain.;VAS (Visual analogue scale);Time to first rescue analgesic.;Onset of sensory block.;Onset of motor block;Sensory recovery time.;Motor recovery time.