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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03091114
Other study ID # V01-A0
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 27, 2017
Est. completion date December 31, 2018

Study information

Verified date October 2018
Source University of Witten/Herdecke
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background:

A predictive factor is a measure that predicts treatment response. Decisions on internal fixations of lower limb fractures should regard predictive factors to personalize (e.g. age) treatment. However for most potentially influencing factors valid data on the predictive value is sparse.

Objectives:

The objective of this study is to identify predictive factors and quantify their predictive ability for treatment failure in patients with limb fractures treated with osteosynthesis.

Methods:

Patients Adult patients (≥18 year) with isolated fractures scheduled for urgent or semi-urgent surgery using internal fixations because of lower limb fractures.

The predictive value of the following exposures will be analyzed:

- Age

- Gender

- Diabetes

- Smoking status

- Body Mass Index

- Open fractures

- Peripheral arterial disease

Outcome The outcome will be (time to) reoperation of the same fracture because of failure of internal fixation due to nonunion or implant failure.

Study design A prospective observational cohort study will be performed. Sample size 300 patients will be included.

Statistical analysis:

For the main analysis a multivariate stratified Cox proportional hazard model will be used. The Model will be stratified according to the indication. In the Cox proportional hazard model all predictive factors will be entered simultaneously to quantify the independent influence (adjusted for all other factors) of each factor. The strength of prediction will be described with hazard rations and their corresponding 95% confidence intervals.


Description:

see study protocol: https://uni-wh.de/fileadmin/user_upload/03_G/07_Humanmedizin/05_Institute/IFOM/IFF-PROFAK_Pro tocol.pdf


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 210
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Adult patients (=18 years) with isolated fractures scheduled for urgent or semi-urgent surgery using internal fixations because of the following lower limb fractures will be included:

- Tibia fractures

- Femur fractures

- Ankle fractures

- Calcaneal fractures

Exclusion Criteria:

- Periprosthetic fractures

- Insufficient knowledge of the German language

- Strong cognitive impairment

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Clinic for orthopedics, trauma surgery and sports traumatology, hospital Cologne Merheim Cologne North-Rhine-Westfalia

Sponsors (1)

Lead Sponsor Collaborator
University of Witten/Herdecke

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Failure of internal fixation Failure of internal fixation due to nonunion or implant failure 6 months +/- 2 weeks (survival analysis)
Secondary Pain Pain numerical rating scale (NRS) >3 6 months +/- 2 weeks
Secondary Physical functioning E.g. climbing stairs 6 months +/- 2 weeks
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