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Comparison between Subarachnoid Block and Lumbar plexus block for Hip and knee surgery

A Comparative Study Between Subarachnoid Block And Lumbar Plexus Block For Hip And Knee Surgery : A Prospective, Randomised Study.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/023054
Enrollment
60
Registered
2020-01-30
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: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Lumbar plexus block: lumbar plexus block in undergoing hip and knee surgery Control Intervention1: subarachnoid block: subarachnoid block in undergoing hip and knee surgery

Sponsors

Government medical college Bhavnagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1-Patients scheduled for elective and emergency knee and hip surgeries(ACL,MM repair, patella TBW, PFN nail, removal of implant etc.) 2-ASA physical status I , II, III . 3-BMI <= 25kg/m2

Exclusion criteria

Exclusion criteria: 1-Spinal deformity. 2-Previous nerve injury. 3-Pre-existing neurological deficit. 4-History of drug allergy (local anesthetics). 5-Patients having altered coagulation profile 6-Local site infection. 7-Psychiatric illness . 8-Any major systemic illness like hypertension, heart block, bronchial asthama etc.

Design outcomes

Primary

MeasureTime frame
1Onset and duration of sensory blockade. 2 Onset and duration of motor blockade. 3 Duration of post operative analgesia. 4 Intraoperative monitoring parameter in term of Heart rate, Mean arterial pressure, spo2 5 Time taken for 1st postoperative analgesic requirement and total analgesic requirement in 1st 24 hour.Timepoint: 24 hour

Secondary

MeasureTime frame
1-Surgeonâ??s satisfaction score. 2-patientâ??s satisfaction score 3- to measure any complicationTimepoint: 12 months

Countries

India

Contacts

Public ContactDr Lopa H Trivedi

Government medical college Bhavnagar

trivedi_lopa@yahoo.in9428009958

Outcome results

None listed

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