Comparison of ropivacaine with adjuvant(fentanyl) in spinal block in delivery by operatio
Phase 4
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated deliveryHealth Condition 2: O- Medical and SurgicalHealth Condition 3: 1- Obstetrics
- Registration Number
- CTRI/2023/09/057961
- Lead Sponsor
- Rabindranath Tagore Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Parturients with ASA physical status grade II.
2. Posted for elective lower segment caesarean section under SAB.
Exclusion Criteria
1. Parturient’s refusal to participate in study.
2. Parturients having coagulation abnormalities, platelet count <70,000, INR >1.5, or on anticoagulants.
3. Parturients having systemic illness (like severe hypovolemia, raised intracranial pressure, neuromuscular diseases, ischemic/ valvular/ congenital heart diseases, psychiatric, hematological disorder).
4. Parturients having any absolute contraindications for spinal anaesthesia.
5. Any allergy to local anaesthetic.
6. Short stature (height <150 cm) and spinal deformity.
7. Morbid obesity (BMI > 40).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesia.Timepoint: Upto 6 hours post-operatively.
- Secondary Outcome Measures
Name Time Method 1. Sensory and motor block characteristics including onset, peak level and duration. <br/ ><br>2. Haemodynamic parameters. <br/ ><br>3. Adverse effects.Timepoint: Upto 24 hours post-operatively.