To study the reduction in analgesia requirement and the quality of recovery after preoperative spinal morphine in patients with pelvic acetabular injuries undergoing stabilisation

To study the reduction in intra- and postoperative analgesia requirement and the quality of recovery after pre-emptive intrathecal morphine in patients with pelvic acetabular injuries undergoing stabilisation surgery

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2015/12/006466

Enrollment

Registered

2015-12-31

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- patients with pelvic acetabular injuries

Interventions

Intervention1: Intrathecal morphine: After induction of general anaesthesia, intrathecal morphine 300 microgram will be given using 27 G spinal needle in L2-3, L3-4 space in lateral position Control I

Eligibility

Inclusion criteria

Inclusion criteria: 18-65 years of age ASA grade I-II undergoing stabilisation for pelvic acetabular injuries

Exclusion criteria

Exclusion criteria: hemodynamic instability (MAP < 60 mm Hg), Polytrauma including head and thoracic injuries, Suspected/ known coagulation abnormalities, sepsis, fever, and anatomically distorted spines

Design outcomes

Primary

Measure	Time frame
Intraoperative analgesia requirement Time to first analgesic Total morphine consumptionTimepoint: Intraoperative period 24 hours postoperative period	—

Secondary

Measure	Time frame
Quality of recovery Adverse effectsTimepoint: Immediate postoperative period 24 hours postoperative period	—

Countries

India

Contacts

Public Contactchhavi sawhney

JPNApex trauma Centre,AIIMS,New Delhi

drchhavisawhney@gmail.com9868397816

Outcome results

None listed

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