A STUDY COMPARING TWO PAIN RELIEF METHODS AFTER ABDOMINAL HYSTERECTOMY SURGERY

Comparison on the effects of epidural levobupivacaine and morphine for post operative analgesia following total abdominal hysterectomy - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/101256

Enrollment

Registered

2026-01-15

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Health Condition 1: C579- Malignant neoplasm of female genital organ, unspecified Health Condition 2: C569- Malignant neoplasm of unspecifiedovary

Interventions

Intervention1: Epidural Levobupivacaine: Patients will receive epidural levobupivacaine 0.25%, 10 mL administered via epidural catheter immediately after completion of surgery for postoperative analge

Eligibility

Inclusion criteria

Inclusion criteria: Scheduled for elective total abdominal hysterectomy. ASA I or II. Consent to participate in the study.

Exclusion criteria

Exclusion criteria: Known allergy to local anaesthetics or opioids. Coagulopathy or local infection at the epidural site. Chronic opioid neurological disorders use or pre-existing neurological disorder. Severe hepatic, renal, or cardiovascular disease.

Design outcomes

Primary

Measure	Time frame
Duration of effective postoperative analgesiaTimepoint: Duration of effective postoperative analgesia	—

Secondary

Measure	Time frame
Postoperative pain intensityTimepoint: VAS at rest and on movement at 2, 4, 8, 12 and 24 hours postoperatively;Requirement of rescue analgesiaTimepoint: Number and total dose of rescue analgesics required within first 24 hours postoperatively;Incidence of adverse effectsTimepoint: Assessed continuously during first 24 hours postoperatively;Patient satisfaction scoreTimepoint: Assessed at 24 hours postoperatively	—

Measure

Time frame

Postoperative pain intensityTimepoint: VAS at rest and on movement at 2, 4, 8, 12 and 24 hours postoperatively;Requirement of rescue analgesiaTimepoint: Number and total dose of rescue analgesics required within first 24 hours postoperatively;Incidence of adverse effectsTimepoint: Assessed continuously during first 24 hours postoperatively;Patient satisfaction scoreTimepoint: Assessed at 24 hours postoperatively

—

Countries

India

Contacts

Public ContactDR Mohammed Yunus Khilji

Sardar Patel Medical College

mohammedyunus.khilji@nhs.net8587858715

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026