Comparison of the effect of adding midazolam, paracetamol, tramadol and magnesium sulphate to ?ropivacaine in reducing pai

Phase 3

Recruiting

• Conditions: Forarm surgery.; Unspecified injury of ulnar artery at forearm level, right arm, sequela; S55.001S

• Registration Number: IRCT20141209020258N168
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 160

Inclusion Criteria

Candidate of forearm surgery
ASA class 1 and 2
No Raynaud's disease
Absence of any vascular disease
No sickle cell anemia
No history of allergy to the drugs used in the study
Lack of cyanosis of the affected limb
Do not use drugs and psychotropic substances
No contraindication to intravenous anesthesia
No more than one fracture in the body or surgery
Absence of chronic pain syndrome
Absence of neurological disorders in the hand

Exclusion Criteria

For any reason, local intravenous anesthesia may be terminated during surgery
Not consent to participate in study
Duration of operation less than 30 minutes or more than 90 minutes

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sensory block. Timepoint: From the beginning study to 24 hours. Method of measurement: Physical examination.;Motor block. Timepoint: From the beginning study to 24 hours. Method of measurement: Physical examination.;Pain. Timepoint: After filling the tourniquet, 15, 30 and 45 minutes after the start of surgery and 30, 60, 90 and 120 minutes after the end of surgery. Method of measurement: Visual analogue pain questionnaire.;Average use opioids. Timepoint: Within 24 hours after surgery. Method of measurement: View file.