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Study of pain relief after surgical delivery of baby

Study of Postoperative Pain Relief After Caesarean Delivery Under Subarachnoid Block

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/01/011097
Enrollment
300
Registered
2018-01-02
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- Lower Segment Caesarean Section

Interventions

None listed

Sponsors

LADY HARDINGE MEDICAL COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy parturients (ASA physical status I and II) scheduled to undergo lower segment Caesarean section under subarachnoid block.

Exclusion criteria

Exclusion criteria: ASA III and IV (Myocardial {NYHA class IIIâ??IV}, severe cerebrovascular, renal or hepatic impairment), refuse subarachnoid block, any contraindication to subarachnoid block (infection at the needle insertion site, spinal deformity, coagulation disorders) or to nerve block or to intramuscular injections, body weight >90Kg or

Design outcomes

Primary

MeasureTime frame
The mean duration of postoperative analgesia, defined as the time (in hours) from the time of giving the analgesic technique to first analgesic request in the postoperative period. Timepoint: 1,3,6,12,24,36 and 48 hrs postoperatively—

Secondary

MeasureTime frame
To study the difference the total amount (mg) of analgesics in the first 48 hours postoperatively in different analgesic techniques, difference in patient satisfaction scores and side effects of drugs used. Timepoint: 1,3,6,12,24,36 and 48 hrs postoperatively—

Countries

India

Contacts

Public ContactKavita Yadav

Lady Hardinge Medical College

ranjusingh1503@yahoo.com9811151285

Outcome results

None listed

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