Study of local anesthetic for caesarean section in pregnant females
Phase 2
- Conditions
- Health Condition 1: O11- -2146826259Health Condition 2: O149- Unspecified pre-eclampsia
- Registration Number
- CTRI/2024/04/065731
- Lead Sponsor
- IMS, BH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Pregnant women with pre-eclampsia undergoing LSCS
Exclusion Criteria
Eclampsia
placenta previa
contraindication of neuraxial block
placental abruption
pulmonary edema and cyanosis
hepatic and renal involvement
BMI more than 35 kg per meter square
height less than 150 cm or more than 180 cm
HELLP syndrome
Multifetal pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method hemodynamic parameter of hyperbaric 0.5% levobupivacaine during perioperative periodTimepoint: 12 months
- Secondary Outcome Measures
Name Time Method onset of sensory block and motor block <br/ ><br>duration of analgesia <br/ ><br>quality of motor blockadeTimepoint: 12 months