ROPIVACAINE FOR SPINAL ANAESTHESIA IN CAESAREAN SECTION

A Study based on Randomised Controlled Trial To Compare The Effects Of 0.5% Bupivacaine (Heavy) With 20 microgram Fentanyl And 0.75% Ropivacaine With 20 microgram Fentanyl For Caesarean Section In Spinal Anaesthesia

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/05/014004

Enrollment

Registered

2018-05-21

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- sensory and motor block after spinal anaesthesia

Interventions

Intervention1: ROPIVACAINE: 0.75% Ropivacaine 2 ml With 20 microgram Fentanyl given as a bolus into subarachnoid space For Caesarean Section In Spinal Anaesthesia Control Intervention1: BUPIVACAINE: 0

Eligibility

Inclusion criteria

Inclusion criteria: 1) elective LSCS 2) ASA 1& 2 3)BMI 4) height between 5 - 6 feet

Exclusion criteria

Exclusion criteria: 1) patient refusal 2) patients with coagulopathy or neuromuscular disease 3) patients on anticoagulants or antiplatelets 4) patients with spine deformity 5) patients with local skin lesion at site of injection 6) known allergy to trial drugs 7) patients with poor myocardial contractility 8) ASA 3 or more 9) emergency lscs

Design outcomes

Primary

Measure	Time frame
SENSORY AND MOTOR BLOCKADETimepoint: EVERY 10 MINUTES AFTER SPINAL ANAESTHESIA UNTIL FIRST ANALGESIC REQUIREMENT	—

Secondary

Measure	Time frame
EFFECT ON HAEMODYNAMICSTimepoint: EVERY 10 MINUTES AFTER SPINAL ANAESTHESIA TILL COMPLETION OF SURGERY	—

Countries

India

Contacts

Public ContactDR APARNA CHANDRAMOHAN

Sree Gokulam Medical College And Research Foundation

drmadhuvelayuden@gmail.com04723041000

Outcome results

None listed

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