Forearm fracture. Other specified acquired deformities of forearm
Conditions
Interventions
Intervention 1: Intervention group: The nitroglycerin group will be injected with 200 micrograms of nitroglycerin (Iran Caspin Company) along with 0.2% ropivacaine. The volume of ropivacaine in all gr
Sponsors
Vice chancellor for research, Arak University Of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 65 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Esmaeel Moshiri
Arak University of Medical Sciences
Outcome results
None listed