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Comparing Surgical Techniques for CRIF of Pertrochanteric Fractures

Comparing Surgical Techniques for CRIF of Pertrochanteric Fractures

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00686023
Enrollment
100
Registered
2008-05-29
Start date
2008-06-30
Completion date
2012-01-31
Last updated
2008-05-29

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

Conditions

Femur Fracture

Keywords

pertrochanteric femur fracture, DHS, IMN

Brief summary

Hypothesis: Inflatable intra medullary femoral nailing is superior to DHS in terms of blood loss, operative complications and postoperative rehabilitation in the management of pertrochanteric femur neck fractures.

Detailed description

patients with pertrochanteric fractures of the femur will be randomly assigned to one of 2 groups. group 1 will undergo internal fixation using a DHS device. group 2 will undergo internal fixation using an inflatable intramedullary femoral nail device post operative care will be the same including DVT prophylaxis, early mobilization. weight baring will be aloud in cases of a stable fracture (EVANS 1-3) non weight bearing until callus bridge in patients with unstable fractures (EVANS 4-6) outcomes: death within first year postoperative complications length of hospitalization time to mobilization functional score reontgenic evaluation

Interventions

PROCEDUREinternal fixation (DHS - richard nail)

internal fixation

PROCEDUREinternal fixation (inflatable PFN by DISCOTEC)

internal fixation

Sponsors

Tel-Aviv Sourasky Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pertrochanteric femur fracture * Unilateral * Age over 60 years * Low energy trauma * ASA score 0-3

Exclusion criteria

* Reverse oblique fractures * Pathological fractures * Severe osteoarthritis of the hip joint * Previous operations on same leg * ASA score 4-5

Design outcomes

Primary

MeasureTime frame
death within 1 year of operation4 years

Countries

Israel

Contacts

Primary ContactEli Steinberg, MD
steinberge@tasmc.health.gov.il972-3-6974727

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026