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Cafeteria approach in Labour Analgesia - Acceptance and Effectiveness among parturients

Cafeteria Approach in Obstetric Analgesia: Acceptance and Effectiveness of Parturient - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/103495
Enrollment
90
Registered
2026-02-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil

Sponsors

Kasturba Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Singleton pregnancy Cephalic presentation Term pregnancy more than 37weeks Women in active labour Cervical dilatation more than 4cm Spontaneous or Induced labour

Exclusion criteria

Exclusion criteria: Contraindications to any of the three analgesic options Known h/o opioid allergy High risk pregnancies (Eg-Pre-eclampsia, thrombocytopenia) Multiple pregnancies Refusal to participate Non-reassuring NST or fetal distress

Design outcomes

Primary

MeasureTime frame
Maternal Pain relief effectivenessTimepoint: From active labour and at 30mins, 1 hour and 2 hours.—

Secondary

MeasureTime frame
Acceptance of each analgesic method Duration of labourTimepoint: 24hours postpartum—

Countries

India

Contacts

Public ContactNandhana V

Kasturba Medical College, Manipal

shyamala.g@manipal.edu9844551037

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026