The effect of adjusted dose of bupivacaine % 0.5 based on height and weight on sensory and motor block in Cesarean sectio
Phase 2
Recruiting
- Conditions
- Spinal anesthesia in cesarean section.Single live born infant, delivered by cesareanZ38.01
- Registration Number
- IRCT20120915010841N12
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
Patient's consent to participate in the study
No history for diabetes, high blood pressure, heart disease
No anemia
Exclusion Criteria
Patients with contraindications of spinal anesthesia (ICP increase, shock, history of coagulation problems ..);
multiple birth;
Weight less than 50 and more than 110 kg.
Height less than 140 and more than 180 cm
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method abour pain. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: visual analgesic scale.;Labour progress. Timepoint: labour duration. Method of measurement: duration of first and second stages of labour.;Systolic and diastolic blood presure. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: non invasive blood pressure monitoring.;Tempreture. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: Termometer.;Quality motor block. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: Bromage scure.;Sensory block quality. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: visual analgesic scale.
- Secondary Outcome Measures
Name Time Method ausea & vomiting. Timepoint: after delivery. Method of measurement: Observation.;Itching. Timepoint: ?? ?? ??????. Method of measurement: Observation &visual scale.;New born Apgar. Timepoint: 1&5 minutes after delivery. Method of measurement: Apgar Score.