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The study to compare efficacy and safety of fractionated versus single bolus dose in spinal anaesthesia in obese parturients undergoing cesarean section.

Prospective observational study to compare efficacy and safety of fractionated versus single bolus dose in spinal anaesthesia in obese parturients undergoing cesarean section. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107370
Enrollment
80
Registered
2026-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: study to compare efficacy and safety of fractionated versus single bolus dose spinal anesthesia in obese parturients undergoing elective cesarean section: The aim of our study is to com

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patients posted for elective cesarean section.patient is able to give informed written consent.obese parturients with BMI above 30.

Exclusion criteria

Exclusion criteria: any contraindication to spinal anaesthesia.[allergy to study drug,local infection,coagulopathy,neurological or cardiac diseases]

Design outcomes

Primary

MeasureTime frame
to compare hemodynamics by comparing systolic,diastolic,mean blood pressure,heart rate and incidence of hypotension ,vasoactive drug required to treat hypotension.Timepoint: patients heart rate, systolic,diastolic,mean arterial pressure are measured every 5 minutes ,till 15 minutes and then at 30 minutes , and at 1 hour,at 1 hour 15 minutes,1hour 30 mins,1 hour 45 mins ,2 hours ,2 hours 30 mins and till end of surgery after giving spinal anesthesia—

Secondary

MeasureTime frame
to compare the peak sensory level achieved,maximum degree of motor block achieved,failure of spinal anaesthesiaTimepoint: spinal block characteristics like sensory level,motor block is assessed every 1 minute till 5 minutes,and every 5 mins till 30 mins,every 15 mins till end of surgery & every 30 minutes until point of regression of sensory level reaches to L1 level.—

Countries

India

Contacts

Public ContactDr Jyoti magar

lokmanya tilak municipal medical college,mumbai,maharashtra,india.

jyotimagar2110@gmail.com9833706466

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026