A Comparison the effects of lidocaine - dexamethasone with Lidocaine -epinephrine intrathecal on quality of sensory block
Phase 2
- Conditions
- Other complications of Anesthesia during pregnancy.Other complications of anaesthesia during pregnancy
- Registration Number
- IRCT201205279874N1
- Lead Sponsor
- Vice-chancellor Of Research Babol University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
elective cesarean section in pregnant women 18-35 years ,ASA ClassI, II ,elective cesarean section
Exclusion criteria from the study: patients with a history of alergy, psychiatric disorder, chronic pain, those taking corticosteroids , alcohol and drug dependence , emergency cesarean
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The duration of sensory block. Timepoint: Every 15 minutes until 4 dermatom regretion. Method of measurement: Pin prik test with needle.;Onset of sensory block. Timepoint: Time from intrathecal injection to highst sensory level. Method of measurement: Pin prik test with needle.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: Every 3 min to end of surgery. Method of measurement: Manometer.;Hear rate. Timepoint: Every 5 min to recovery. Method of measurement: ECG.;Nausea. Timepoint: During delivery to24 hours. Method of measurement: Questioning from patient(having or not).;Vomiting. Timepoint: During delivery to 24 hours. Method of measurement: Questiening from patient.;Pain. Timepoint: Recovery room to 24 hours. Method of measurement: Visual analog scale.