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Prospective randomised double blind study between the efficacy of intrathecal 0.5% heavy vs isobaric Bupivacaine in elective LSCS.

Prospective Randomized double blind comparitive study between the efficacy of intrathecal 0.5 percent Bupivacaine heavy vs isobaric in elective lscs. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085023
Enrollment
48
Registered
2025-04-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Injection Bupivacaine 0.5 percent isobaric.: Isobaric Injection Bupivacaine 0.5 percent 2.0 ml to be given as drug for spinal anaesthesia in patients undergoing elective lower section c

Sponsors

dy patil school of medicine and hospital nerul navi mumbai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 All patients giving consent undergoing elective lscs 2 ASA grade 2 3 patients coming for elective c-section with gestational age og greater than 35 weeks 4 height more than 150 cms

Exclusion criteria

Exclusion criteria: Patients undergoing emergency C-SECTIONS 1 Patients known or suspected to have allergy for study drugs. 2 Patient refusal 3 Patients with contraindications to spinal anaesthesia.

Design outcomes

Primary

MeasureTime frame
To compare the anaesthetic properties of isobaric and hyperbaric bupivacaine in spinal anaesthesia, which includes the time of onset of sensory and motor block and duration of block obtained (both sensory and motor)Timepoint: at base line,2 mins,4 mins, 6 mins, 8 mins, 15 mins, 20 mins, 25 mins, 30 mins, 40 mins, 50 mins, 60 mins

Secondary

MeasureTime frame
To compare the effects of both the drugs on haemodynamic parameters which include heart rate & blood pressure & side effects.Timepoint: at 2 minutes,4 minutes,6 minutes, 8 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, 30 minutes, 40 minutes, 50 minutes , 60 minutes after the induction of spinal anaesthesia

Countries

India

Contacts

Public ContactDr Balasaheb Govardhane

D.Y Patil school of medicine

gbalasaheb690@gmail.com9819631719

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026