The prophylactic effect of neostigmine and atropin combination on the occurrence of post-dural puncture headache in patients undergoing spinal anesthesia
Phase 3
Recruiting
- Conditions
- ower limb surgery.Unspecified injury of left lower leg, initial encounterS89.92XA
- Registration Number
- IRCT20200825048515N11
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Patient consent to participate in the study
American Anesthesiologists Association Classification I and II
Duration of surgery less than 2 hours
Exclusion Criteria
Taking anticoagulants
Existence of a nerve lesion in the limb/spine
Coagulation diseases
History of spinal surgery, spinal canal stenosis
Conductive disorders of the heart
History of migraine headaches
Opioid addiction
History of malignancy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain severity. Timepoint: From first day to seven days after surgery. Method of measurement: Visual Analogue Scale (VAS).;Duration of headache. Timepoint: From first day to seven days after surgery. Method of measurement: Counting the number of days suffering from headache.
- Secondary Outcome Measures
Name Time Method