Spinal anesthesia in cesarean sectio
- Conditions
- Health Condition 1: 1- ObstetricsHealth Condition 2: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2018/10/016106
- Lead Sponsor
- Dr S N Medical College Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
INCLUSION CRITERIA:
1.Patients belonging to age group 18-35 years.
2.American Society Of Anaesthesiologists(ASA) grade 1 and 2.
3.Body Mass Index (BMI) between 20-35 kg/m2.
4.Patients undergoing elective caesarean section.
1.Patients refusal
2.Known hypersensitivity to local anaesthetics
3.Patients with infection at the site of infection
4.ASA grade 3 & 4 patients
5.Patients with history of bleeding disorders or patients on anticoagulants
6.Parturient with pregnancy induced hypertension
7.Emergency delivery
8.BMI >35kg/m2
9.Patients with cardiac disease (like heart blocks, dysarrythmias), renal or other organ system disease which preclude choice of spinal anaesthesia.
10. Pre existing peripheral neuropathy or neurological deficit or psychiatric disease
11. Anatomical abnormality
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesia.Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method 1.To assess onset and duration of sensory block . <br/ ><br>2. To assess onset and duration of motor block . <br/ ><br>3.To assess the level of sensory block. <br/ ><br>4.To assess the level of motor block. <br/ ><br>5. Consumption of analgesic in first 24 hrs. <br/ ><br>6.To compare haemodynamics and respiratory parameters. <br/ ><br>7.Quality of block. <br/ ><br>8.Neonatal outcome(APGAR SCORE) <br/ ><br>9.Patient satisfaction. <br/ ><br>10.Any side effects or complications including TNS <br/ ><br>Timepoint: upto 6 months