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A prospective randomized-controlled trial study to study the duration of Post operative analgesia of a combination of Low Dose Spinal Anaesthesia and Lumbar and Sacral Plexus Blocks in Lower Limb Surgery

A prospective randomized-controlled trial study to study the duration of Post operative analgesia of a combination of Low Dose Spinal Anaesthesia and Lumbar and Sacral Plexus Blocks in Lower Limb Surgery - Nil

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/077717
Enrollment
40
Registered
2024-12-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: S729- Unspecified fracture of femur

Interventions

Intervention1: Low Dose Spinal with lumbar and sacral plexus blocks: Duration of post operative analgesia Control Intervention1: Combined Spinal Epidural: Duration of post operative analgesia Visual A

Sponsors

Vikhe Patil Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing lower limb surgeries including trauma surgery 2. Age above 18

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of post operative analgesiaTimepoint: Duration of post operative analgesia—

Secondary

MeasureTime frame
Analgesic requirementTimepoint: 48 hours—

Countries

India

Contacts

Public ContactDr Nikhil Karkhanis

Vikhe Patil Institute of Medical Sciences

nikhilkarkhanis@rediffmail.com9977000738

Outcome results

None listed

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