A study to compare between lumbar plexus block with low spinal anesthesia with conventional spinal anesthesia for hip surgeries

A COMPARATIVE STUDY BETWEEN THE LUMBAR PLEXUS BLOCK AND LOW SPINAL WITH CONVENTIONAL SPINAL ANESTHESIA IN HIP SURGERIES

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/01/039280

Enrollment

Registered

2022-01-10

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Lumbar plexus block with low spinal: lumbar plexus block given using peripheral nerve stimulator with 10ml of 0.5% Bupivacaine and 15ml of plane 2% lignocaine low spinal anesthesia usin

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients undergoing elective HIP surgeries 2.Between the ages of 20-80 years, of either sex 3.ASA (American society of anaesthesiologists) grade I,II and III 4.BODY WEIGHT 50-90KG

Exclusion criteria

Exclusion criteria: 1.Patients with ASA (American society of anaesthesiologists) grade IV. 2. Patients who have known allergies to local anaesthetics drugs. 3. Patients with coagulation disorders or on anti coagulant drugs.

Design outcomes

Primary

Measure	Time frame
1.To study the hemodynamic stability and anaesthetic effects of lumbar plexus block and low spinal with conventional spinal anaesthesia perioperatively in hip surgeries. 2.To study the complications of the above techniques in the perioperative period. 3.To compare the postoperative analgesia in the above techniques Timepoint: 24 hours	—

Secondary

Measure	Time frame
1. to study any complication associated with the two techniques 2.compare comfortability of the patients with 2 techniquesTimepoint: 5 days	—

Countries

India

Contacts

Public ContactDr Ajay kumar

Mahadevappa rampure medical college

murthykaja@gmail.com8762068682

Outcome results

None listed

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