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Comparison of two spinal anesthesia drugs, levobupivacaine and ropivacaine, in cesarean section surgeries

Comparison of effectiveness of intrathecal injection of levobupivacaine and ropivacaine in lower section cesarean section surgeries : A randomised double blind prospective comparative control clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107497
Enrollment
72
Registered
2026-04-02
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: O- Medical and Surgical

Interventions

Intervention1: Spinal Anaesthesia intrathecal injection: Spinal anesthesia also called as Subarachnoid block is the preferred technique for lower section cesarean section, avoiding complications relat

Sponsors

Shantabaa medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American society of anaethseiologists physical status 1 & 2. Patients scheduled for elective cesarean section. Informed consent obtained for participation in the study.

Exclusion criteria

Exclusion criteria: Patient refusal. Patients with allergies to local anesthetics Patients with a history of chronic neurological disorders. Patients with contraindications to regional anaesthesia e.g. infection at the injection site, patients with altered coagulation profiles/any bleeding diathesis, significant cardiovascular disease)

Design outcomes

Primary

MeasureTime frame
Duration of sensory block, defined as time from intrathecal injection to L1 level regression from highest achieved sensory level.Timepoint: timeframe and duration of sensory block, defined as time from intrathecal injection to L1 level regression from highest achieved sensory level. approximately upto 2-4 hours post spinal intrathecal injection

Secondary

MeasureTime frame
Duration of motor block , defined as time from intrathecal injection to achievement of modified bromage grade 3 to regression to modified bromage grade 1Timepoint: Motor block will be assessed at baseline (pre-spinal), then every 2 minutes after intrathecal injection until Modified Bromage grade 3 is achieved, & thereafter every 15 minutes until regression to Modified Bromage grade 1 (up to approximately 2 5 hours post spinal anesthesia).

Countries

India

Contacts

Public ContactDr Ravikumar M Parnar

Shantabaa medical college

Ravirajparmar1@gmail.com9099097807

Outcome results

None listed

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