The effect of Sprotte or Quincke spinal needles on the frequency and severity of transient neurologic syndrome
Not Applicable
Recruiting
- Conditions
- The effect of Sprotte and Quincke spinal needles on the frequency and severity of neurological syndrome.Other complications of spinal and epidural anesthesia during labor and deliveryO74.6
- Registration Number
- IRCT20110712007013N26
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 160
Inclusion Criteria
Candidate for elective cesarean delivery
Candidate for spinal anesthesia
Patients between 18-40 years ASA Class I&II
Term and singleton pregnancy
Exclusion Criteria
Weight over 100 kg and height less than 150 cm
Allergy to local anesthetics medicines
History of psychiatric disease
Spinal cord stenosis and lumbar discopathy
History of systemic diseases (cardiovascular, hepatic, pulmonary, ...)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of onset of symptoms of transient neurological syndrome. Timepoint: 6 to 48 hours after surgery. Method of measurement: Physical examination.;Duration of symptoms of transient neurological syndrome after recovery from anesthesia. Timepoint: 6 to 48 hours after surgery. Method of measurement: Physical examination.;Severity of pain caused by transient neurological syndrome. Timepoint: 6 to 48 hours after surgery. Method of measurement: Similar verbal scoring.
- Secondary Outcome Measures
Name Time Method Type of treatment used for transient neurological syndrome. Timepoint: 6 to 48 hours after surgery. Method of measurement: Clinical record.;The dose of treatment used to treat transient neurological syndrome. Timepoint: 6 to 48 hours after surgery. Method of measurement: Clinical record.