Comparison of two different drugs for spinal anaesthesia in parturients undergoing caesarean sections
Not Applicable
Completed
- Registration Number
- CTRI/2018/12/016660
- Lead Sponsor
- Sapthagiri institute of medical sciences and research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
parturients with gestational age of 37 to 42 weeks having singleton pregnancy with average height of 150 to 170 cms, coming for elective caesarian section
Exclusion Criteria
Parturients with contraindications to spinal anaesthesia, known allergy to local anaesthetics, other medical illnesses like diabetes, pregnancy induced hypertension, hypothyroidism, severe anaemia( <7gm/dl)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effects on duration of postoperative analgesia based on visual analogue scale and onset and duration of motor and sensory anaesthesia based on Bromage grading and blunt tip pin prick sensationTimepoint: 12 hours postoperatively
- Secondary Outcome Measures
Name Time Method Effects on haemodynamic stability and any side effectsTimepoint: 12 hours postoperatively