Effect of rhBMP-2 or rhBMP-7 on Long Bone Fractures and Non-unions.

Sponsor
University Hospital Muenster (Other)
Overall Status
Completed
CT.gov ID
NCT05065684
Collaborator
(none)
150
84

Study Details

Study Description

Brief Summary

Delayed fracture healing continues to cause significant patient morbidity and economic burden to society. Biological stimulation of acute fractures and non-unions includes application of rhBMP-2 and rhBMP-7. However, BMP use continues to be a matter of controversy as literature shows scarce evidence for treatment effectiveness. The aim of this study is to compare acute fractures and non-unions in the long bones humerus, femur and tibia with and without BMP treatment of acute fractures. Furthermore, the investigators want to identify complications and risk factors on union-rate and time to union.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Primary Objective:

    The primary objective is to assess time to union and union rate after rhBMP-2 and rhBMP-7 application at long bone fractures and non-unions.

    Secondary Objective(s):
    • Analysis of secondary complications

    • Analysis of risk factors

    Hypothesis and Statistical considerations and estimated enrollment:

    The investigators hypothesize that with the use of rhBMP-2 and rhBMP-7 there will be a faster timer to union and higher union rate compared to no-BMP. Outcomes will be assessed prospectively.

    This study is exploratory in nature. Therefore, there is no formal statistical hypothesis and no formal sample size calculation. Approximately 150 long-bone fractures and non-unions are expected.

    Data will be analyzed with the use of simple summary statistics. Depending on the volume and quality of the collected data, different statistical analyses will be applied. Exploratory analyses will be conducted to investigate relationships between the different treatment options and the outcomes.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    150 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Effect of rhBMP-2 or rhBMP-7 on Long Bone Fractures and Non-unions.
    Actual Study Start Date :
    Jan 1, 2005
    Actual Primary Completion Date :
    Jan 1, 2012
    Actual Study Completion Date :
    Jan 1, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    rhBMP-2 and rhBMP-7

    patients who have been treated with rhBMP-2 or rhBMP-7 for long bone non-union or acute fractures

    No-BMP

    patients who have been treated with standart care, i.e. non-union resection and autologous bone graft

    Outcome Measures

    Primary Outcome Measures

    1. Time to Union [24 months]

      Time to Union in months

    2. Union-rate [24 months]

      Union-rate in percentage

    Secondary Outcome Measures

    1. Risk factor analysis [24 months]

      Clinically relevant retrospective data regarding medical history, co-morbidity, the localization and the outcome will be collected. Comorbidities are listed and categorized as follows: Cardiovascular (peripheral arterial disease, hyperuricemia, coronary artery disease, bleeding disorders, hemophilia A, thrombocytopenia, blood loss anemia), metabolic (diabetes, adiposities, hypertonia, metabolic syndrome, liver disorders, alcoholic liver cirrhosis, alcohol abuse, hypothyroidism, hyperkalemia), neurologic (Parkinson, borderline personality, suicidality, epilepsy, drug abuse, sleep apnea syndrome, status post apoplexy), rheumatologic and allergic (atopic eczema, rheumatoid arthritis, bronchial asthma, chronic bronchitis) and infectious (MRSA, hepatitis A, B and C).

    2. complications/Adverse Events related to implant or surgery [24 months]

      complications/Adverse Events related to implant or surgery

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Long bone fracture or long bone non-union.

    • Signed informed consent, if required by IRB/EC

    Exclusion Criteria:

    Prisoner at date of inclusion

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University Hospital Muenster

    Investigators

    • Principal Investigator: Michael J. Raschke, Prof. Dr., University Hospital Muenster

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital Muenster
    ClinicalTrials.gov Identifier:
    NCT05065684
    Other Study ID Numbers:
    • Effect of rhBMP-2 or rhBMP-7
    First Posted:
    Oct 4, 2021
    Last Update Posted:
    Oct 4, 2021
    Last Verified:
    Aug 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Hospital Muenster
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 4, 2021