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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 encounter
S89.92XA
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
NameTimeMethod
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
NameTimeMethod
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