a study to compare two drugs preventing decrease of blood pressure in elective cesarean sectio
Not Applicable
Completed
- Conditions
- Health Condition 1: null- ASA 1 and 2 pregnent female
- Registration Number
- CTRI/2017/09/009638
- Lead Sponsor
- nil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
ASA grade 1 and 2
Weight 40 to 80 kg
pregnant female posted for elective cesarean section
Exclusion Criteria
Patients not willing to participate in the study.
Uncooperative patients.
Any known hypersensitivity or contraindication to bupivacaine , fentanyl,noradranaline,phenylephrine.
Local pathology at the site of injection or disability limiting the performance of spnal anaesthesia.
Patient have any associated co-morbidity
onset of labor,
known fetal abnormality,
Inadequate effect of spinal anaesthesia or those converted in genral anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean arterial pressure <br/ ><br>Cardiac output <br/ ><br>Heart rate <br/ ><br>Stroke volume <br/ ><br>Systemic vascular resistence <br/ ><br>Timepoint: two hours <br/ ><br>
- Secondary Outcome Measures
Name Time Method eonatal APGAR score <br/ ><br>Timepoint: five min