Bupivacaine effect on transient neurologic syndrome after cesarean sectio
Phase 2
- Conditions
- Epidural analgesia quality.Other complications of spinal and epidural anaesthesia during labour and delivery
- Registration Number
- IRCT201612237013N16
- Lead Sponsor
- Tabriz Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other
- Sex
- Male
- Target Recruitment
- 230
Inclusion Criteria
pregnant women candidate for cesarean section under epidural analgesia; Class I or II according to ASA classification.
Exclusion criteria: contraindications for epidural analgesia; sensitivity to local analgesics; history of neurovascular or neuromuscular diseases; history of diabetes; history of mental disorders; intervertebral disc hernia or spinal stenosis; lower extremity neuropathy.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of TNS symptoms onset. Timepoint: 6 to 48 hours after operation. Method of measurement: physical examination.;Duration of TNS symptoms after analgesia recovery. Timepoint: 6 to 48 hours after operation. Method of measurement: physical examination.;Pain severity due to TNS. Timepoint: 6 to 48 hours after operation. Method of measurement: visual analogue scale.
- Secondary Outcome Measures
Name Time Method Type of treatment used to treat TNS. Timepoint: 6 to 48 hours after operation. Method of measurement: clinical document.;Dosage of treatment used for TNS recovery. Timepoint: 6 to 48 hours after operation. Method of measurement: clinical document.