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Comparison of fascia iliaca compartment block or femoral nerve block using levobupivacaine for postoperative analgesia after operative repair of femoral neck fracture: a dose response study - FICB/FNB for fractured NOF: A dose response study

Comparison of fascia iliaca compartment block or femoral nerve block using levobupivacaine for postoperative analgesia after operative repair of femoral neck fracture: a dose response study - FICB/FNB for fractured NOF: A dose response study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2009-013134-24-GB
Enrollment
Unknown
Registered
2009-06-12
Start date
2009-07-31
Completion date
Unknown
Last updated
2012-03-19

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

Conditions

Postoperative Analgesia in patients undergoing operative repair of fractured neck of femur

Interventions

Trade Name: 0.5% Chirocaine Product Name: LEVOBUPIVACAINE Pharmaceutical Form: Solution for injection

Sponsors

Belfast Health & Social Care Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria for subjects i) ASA class I-III (American Society Of Anesthesiologists Grading) ii) Patients able to give written informed consent iii) Patients requiring operative repair of fractured neck of femur Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Exclusion criteria i) History of allergy to any of the medications used in the study ii) Patients with a history of dementia or difficulty in providing informed consent iii) Patients with a history of significant neurological impairment of one or both of the lower limbs iv) Patients with a pathological fracture of the neck of femur v) Patients suffering from severe hypotension such as cardiogenic or hypovolaemic shock or with a serious cardiac arrhythmia

Design outcomes

Primary

MeasureTime frame
Main Objective: Comparison of postoperative pain scores after one of two nerve blocks using one of two doses of the local anaesthetic following operative repair of fractured neck of femur. ;Secondary Objective: Secondary end points (i) Incidence of motor blockade (ii) Postoperative analgesia requirements and time to first request of postoperative analgesia (iii) Ability to mobilise on the first postoperative day (iv) Incidence of any adverse events ;Primary end point(s): Comparison of postoperative pain scores after one of two nerve blocks using one of two doses of the local anaesthetic following operative repair of fractured neck of femur.

Countries

United Kingdom

Outcome results

None listed

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