The effect of rocuronium and nitroglycerin in reducing pain in intravenous local anesthesia

Phase 2

• Conditions: Forearm fracture.; Other specified acquired deformities of forearm; M21.83

• Registration Number: IRCT20141209020258N183
• Lead Sponsor: Vice chancellor for research, 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 May 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 177

Inclusion Criteria

20-65 years
ASA class I and II
Forearm surgery candidate
Consent to enter the study
Not having Raynaud's disease
Not having sickle cell anemia
No history of allergy to the drugs used in the study
Absence of cyanosis of the affected organ
No use of drugs and psychotropic substances
No contraindications for intravenous anesthesia
The absence of more than one fracture in the body or surgery
Absence of chronic pain syndrome
Absence of neurological disorders in the hand

Exclusion Criteria

The duration of surgery is more than 90 minutes
For any reason, the local intravenous anesthesia is terminated (ineffective) during the operation.
The duration of the operation is less than 30 minutes

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: After filling the tourniquet, and at times 15, 30 and 45 and every 15 minutes until the end of the surgery, after emptying the tourniquet every 30 minutes up to 2 hours (minutes 30, 60, 90 and 120) and then every two hours until 12 hours (4, 6, 8, 10 and 12 hours) after emptying the tourniquet. Method of measurement: Visual analog scale of pain.