Evaluation of the effect of adding dexamethasone to lidocaine in digital block
Phase 2
Recruiting
- Conditions
- Digital nerve block.
- Registration Number
- IRCT20110103005536N9
- Lead Sponsor
- Artesh University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
All patients 20 to 60 years
ASA |
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.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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).
- Secondary Outcome Measures
Name Time Method