A Randomized Control Trial Comparing Pain Profiles After Combined Peripheral Nerve Blocks Versus Spinal Anaesthesia For Proximal Femoral Nailing

A randomised controlled trial comparing pain profiles after Combined peripheral nerve block versus spinal anaesthesia for proximal femoral nailing

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/05/025207

Enrollment

Registered

2020-05-15

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: M848- Other disorders of continuity of bone

Interventions

Intervention1: Peripheral nerve blocks: Peripheral nerve blocks are used for proximal femoral nailing Control Intervention1: Spinal Anaesthesia: Spinal Anaesthesia is used for proximal femoral nailing

Eligibility

Inclusion criteria

Inclusion criteria: ASA status I to III 60 to 100 years of age Weight 35 TO 70 Kg

Exclusion criteria

Exclusion criteria: Contraindication to regional anaesthesia Preference for regional Anaesthesia Neurological disorder affecting the lower extremities Lack of competence to consent

Design outcomes

Primary

Measure	Time frame
Time of request for first rescue analgesia after the intervention is calculated from the time onset of sensory block Total dose of rescue analgesia in first 24 hoursTimepoint: 18 months	—

Secondary

Measure	Time frame
Post operative quality of recovery scale at 24 hours -Based on Quality of Recovery Scale QoR 15 Scores Need for ICU admission Length of hospital stay-Number of daysTimepoint: 18 Months	—

Countries

India

Contacts

Public ContactUsha Shenoy

Jubilee Mission Medical College Hospital and Research Institute East fort Thrissur

rssuss@gmail.com9446575724

Outcome results

None listed

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