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CLINICAL TRIAL ON LABOUR ANALGESIA

â??EFFECT OF ADDITION OF NEOSTIGMINE ON DOSE REQUIREMENTS OF ROPIVACAINE 0.1% AND DURATION OF LABOUR DURING EPIDURAL LABOUR ANALGESIAâ??

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/013720
Enrollment
56
Registered
2018-05-07
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- Primigravida in labour with gestational age â?¥ 36 weeks

Interventions

Intervention1: Lumbar Epidural analgesia with Ropivacaine with fentanyl and neostigmine: Lumbar Epidural analgesia administered with inj. Ropivacaine, 0.1% with inj.fentanyl 20 mcgm and inj.Neostigmi

Sponsors

Vijayanagar Institute of Medical Sciences Ballari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ) Consenting primigravida in labour, gestational age >= 36 weeks 2) Age 18-35 yrs, singleton pregnancy with vertex presentation

Exclusion criteria

Exclusion criteria: 1) Significant coagulopathy or other contraindications to epidural analgesia 2) ASA III and above 3) Patients with history of significant disorders (Pregnancy induced hypertension, diabetes mellitus, obstetric hemorrhage, other cardiovascular, respiratory, central nervous system or renal system disorders) 4) Allergy to any study drugs

Design outcomes

Primary

MeasureTime frame
To determine total dose requirement of Ropivacaine per hour with addition of neostigmine during epidural labour analgesia Timepoint: To determine total dose requirement of Ropivacaine per hour with addition of neostigmine during epidural labour analgesia at the end of the study

Secondary

MeasureTime frame
To determine : - Duration of labour (in hour) - Labour Outcomes: Spontaneous or instrumental vaginal delivery / Cesarean section - Foetal outcomes: in terms of APGAR score - Maternal hemodynamic changes: HR,SBP,DBP,MABP - Maternal satisfaction: Excellent/Good/fair Timepoint: After the delivery of the patient, determination of : - Duration of labour (in hour) - Labour Outcomes: Spontaneous or instrumental vaginal delivery / Cesarean section - Foetal outcomes: in terms of APGAR score - Maternal hemodynamic changes: HR,SBP,DBP,MABP - Maternal satisfaction: Excellent/Good/fair

Countries

India

Contacts

Public ContactDr Balasubramanya H

VIMS, Ballari

archanadande7@gmail.com9739185610

Outcome results

None listed

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