FindTrial
Sign In

comparison between two techniques of labour analgesia

comparison of combined spinal epidural(f & r) with epidural(continuous infusion of f&r) for labour analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046613
Enrollment
44
Registered
2022-10-19
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery Health Condition 2: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: combined spinal epidural labour analgesia: in combined spinal epidural patients will receive 25microgram opioid through spinal needle intrathecal and local anaesthetic through epidural

Sponsors

Department of anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patients of 18 to 40 yrs of age with a singleton fetus in cephalic presentation at term with 3 to 5 cm of cervical dilatation who will request labour analgesia with no contraindication

Exclusion criteria

Exclusion criteria: patient refusal coagulation disorder non vertex presentation raised ict

Design outcomes

Primary

MeasureTime frame
onset of analgesia after interventionTimepoint: 2 to 3 months—

Secondary

MeasureTime frame
patient satisfaction quality of analgesiaTimepoint: 2 to 3 months—

Countries

India

Contacts

Public ContactDurgesh agrawal

Sardar patel medical college

sonaligsoni@gmail.com9414137866

Outcome results

None listed

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