NCT Number: NCT02657902
Does an Additional Antirotation U-Blade (RC) Lagscrew Improve Treatment of AO/OTA (Orthopaedic Trauma Association) 31 A1-3 Fractures With Gamma 3 Nail?
The purpose was to evaluate whether the additional use of the Gamma3 ® RC Lag Screw is associated with a reduced cutout rate in patients with OTA/AO 31A1-3 inter-trochanteric fractures.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- OTA/AO 31A1-3 fractures treated with Gamma 3® Nail (Stryker Trauma Germany) and either with standard lagscrews or with the Gamma3 ® RC Lag Screw (Stryker Trauma Germany)
Exclusion criteria
- Patients with pathological fractures
- Patients treated with a long gamma nail were excluded
Treatment and study plan
Fractures were treated with a Gamma 3 intramedullary nail + U-Blade
ProcedurePrimary outcomes
-
Cutout rate
Time frame: 3 months after intervention
Differences in the Cutout rate of the femoral head screw with/without U-Blade antirational screw
Secondary outcomes
-
Mobility
Time frame: 3 months after intervention
Mobility of the patients 3 months after intervention measured with the Parker mobility score
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Lead sponsor
Medical University of Vienna
Other
Registry information
Official study title
Does an Additional Antirotation U-Blade (RC) Lagscrew Improve Treatment of AO/OTA (Orthopaedic Trauma Association) 31 A1-3 Classified Fractures With Gamma 3 Nail?
Important dates
- Study start
- 2009
- Primary completion
- 2015
- First posted
- Jan 18, 2016
- Registry last updated
- Jan 18, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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