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Painless delivery

COMPARATIVE EVALUATION OF 0.2% ROPIVACAINE VS 0.125% ROPIVACAINE UNDER COMBINED SPINAL EPIDURAL TECHNIQUE FOR LABOUR ANALGESIA

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/06/014565
Enrollment
60
Registered
2018-06-18
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- ASA grade I and II

Interventions

Intervention1: COMPARATIVE EVALUATION OF 0.2% ROPIVACAINE VS 0.125% ROPIVACAINE UNDER COMBINED SPINAL EPIDURAL TECHNIQUE FOR LABOUR ANALGESIA: It is comparison between different concentratio

Sponsors

Govt Medical College Amritsar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant women with singleton pregnancy, term gestation, cephalic presentation, in active stage of labour, having full term live foetus. Primigravida, without any obstetric complications and requesting for pain relief Having regular contractions at least once every 5 minutes Cervical dilation of 3-4 cm ASA Grade I and II Age 20-35 years Height > 145 cm BMI 18-25 (weight/height2)

Exclusion criteria

Exclusion criteria: 1. Patientâ??s refusal 2. ASA Grade III and IV 3. Coagulation disorders and Bleeding disorders 4. Raised intracranial tension 5. Hypersensitivity to the study drugs 6. Cephalopelvic disproportion (CPD) 7. Pre-term gestation (gestational age 8. Any Vertebral column deformity and spine surgery 9. Any sign of infection at puncture site or sepsis 10. Contraindication for epidural catheter placement 11. Non reassuring NST 12. Foetal weight 4500 gm 13. Multiple pregnancy and malpresentation 14. History of drug abuse and any obstetric complications 15. History of cardiac arrhythmias or labile hypertension

Design outcomes

Primary

MeasureTime frame
Onset of sensory and motor block Duration of sensory and motor block Timepoint: Onset of sensory and motor block Duration of sensory and motor block

Secondary

MeasureTime frame
Maternal and foetal outcome Maternal satisfaction score Side effects and complications Timepoint: 48 hours

Countries

India

Contacts

Public ContactDr Puneetpal Kaur

Govt Medical College, Amritsar

rkhetarpal9@hotmail.com9815654332

Outcome results

None listed

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