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Thigh block for post operative pain management after total hip arthroplasty operation

Fascia iliaca compartment block for postoperative pain management after total hip arthroplasty in a tertiary care hospital-a randomised study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025903
Enrollment
64
Registered
2020-06-16
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: V00-Y99- External causes of morbidity

Interventions

Intervention1: 2% ropivacaine for FICB: 2%ropivacaine 30 ml,once,post operative analgesia Control Intervention1: standard treatment of care: tramadol 100 mg in 100 ml NS tds

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2, Patient willing to participate Patients with indication for THR

Exclusion criteria

Exclusion criteria: ASA 3 and 4 Patients refusing to participate Pregnant woman Patients having allergy to local anaesthetics Failed subarachnoid block

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of the FICB after hip arthroplasty surgery for pain relief during the post operative periodTimepoint: The pain scores will be assessed in 6,8,12hours post surgery—

Secondary

MeasureTime frame
To evaluate for early rehabilitation following hip arthroplasty surgeriesTimepoint: Post operative and follow-up upto 3 weeks post surgery—

Countries

India

Contacts

Public ContactAmrita panda

Kalinga institute of medical sciences

amrita.panda@kims.ac.in9439862335

Outcome results

None listed

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