Digital nerve block.
Conditions
Interventions
Intervention 1: Intervention group: In one group,depending on the color of the patient's black or white card, participating in the project of 3 cc of 2% lidocaine plus 1 cc (equivalent to 4 mg) of dex
Sponsors
Artesh University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: All patients 20 to 60 years ASA |
Exclusion criteria
Exclusion criteria: History of allergy to local anesthetic pregnancy People with a history of diabetes or uncontrolled liver and kidney disease People with hemodynamic instability people with history of peptic ulser People on long-term treatment with corticosteroids.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| FPP (Free Pain Period). Timepoint: When the patient requests an analgesic. Method of measurement: Duration of the patient's analgesic period in hours.;Intensity of pain. Timepoint: During the intervention. Method of measurement: According to the instruction given to all patients on how to express pain intensity according to the equivalent of visual equivalent (Visual Analogue Scale) through a 100 mm ruler, patients express their pain intensity as grade I=30 (mild pain) and grade <30 II=70 (Moderate pain) Grade III is divided into <70 (severe pain). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohamadreza Rafiei
Artesh University of Medical Sciences
Outcome results
None listed