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Evaluation of the Clinical Effectiveness of Bioactive Glass (S53P4) in the Treatment of Tibia and Femur Non-unions

Primary Purpose

Pseudoarthrosis of Bone

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
bioglass (S53P4)
RIA and TCP
Sponsored by
Sebastian Findeisen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pseudoarthrosis of Bone

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • pseudarthrosis of the tibia or femur
  • bone defect < 5 cc
  • surgical treatment with Masquelet technique

Exclusion Criteria:

  • age under 18
  • disagreement
  • patients who require amputation of the affected limb

Sites / Locations

  • University Hospital HeidelbergRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Masquelet technique: bioactive glass

Masquelet technique: RIA + TCP

Arm Description

Outcomes

Primary Outcome Measures

Rate of participants with osseus consolidation evaluation via x-ray
x-ray in 2 planes; union = cortical bridging of at least three out of four cortices

Secondary Outcome Measures

12-item Short Form Survey (SF-12)
Quality of life: Physical Score 23.99938(lowest/worst)-56.57706(highest/best), Mental Score 19.06444(lowest/worst)-60.75781 (highest/best)
Perfusion
Real-time microperfusion assessment using Contrast enhanced ultra-sound (CEUS), contrasting agent: SonoVue. Objective perfusion quantification (using VueBox). Evaluation of characteristic perfusion parameters such as: wash-in rate, wash-in perfusion index
Rate of participants with osseus consolidation evaluation via CT
union = cortical bridging of at least three out of four cortices

Full Information

First Posted
June 8, 2021
Last Updated
September 9, 2021
Sponsor
Sebastian Findeisen
Collaborators
Bonalive Biomaterials Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT05049915
Brief Title
Evaluation of the Clinical Effectiveness of Bioactive Glass (S53P4) in the Treatment of Tibia and Femur Non-unions
Official Title
Evaluation of the Clinical Effectiveness of Bioactive Glass (S53P4) in the Treatment of Non-unions of the Tibia and Femur: a Randomized Controlled Non-inferiority Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sebastian Findeisen
Collaborators
Bonalive Biomaterials Ltd

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Abstract Background: Treatment of non-union remains challenging and often necessitates augmentation of the resulting defect with an autologous bone graft (ABG). ABG is limited in quantity and its harvesting incurs an additional surgical intervention leaving the risk for associated complications and morbidities. Therefore, artificial bone graft substitutes that might replace autologous bone are needed. S53P4-type bioactive glass (BaG) is a promising material which might be used as bone graft substitute due to its osteostimulative, conductive and antimicrobial properties. In this study, the investigators plan to examine the clinical effectiveness of BaG as a bone graft substitute in Masquelet therapy in comparison with present standard Masquelet therapy using an ABG with tricalciumphosphate to fill the bone defect. Methods/design: This randomized controlled, clinical non-inferiority trial will be carried out at the Department of Orthopedics and Traumatology at Heidelberg University. Patients who suffer from tibial or femoral non-unions with a segmental bone defect of 2-5 cm and who are receiving Masquelet treatment will be included in the study. The resulting bone defect will either be filled with autologous bone and tricalciumphosphate (control group, N = 25) or BaG (S53P4) (study group, N = 25). Subsequent to operative therapy, all patients will receive the same standardized follow-up procedures. The primary endpoint of the study is union achieved 1year after surgery. Discussion: The results from the current study will help evaluate the clinical effectiveness of this promising biomaterial in non-union therapy. In addition, this randomized trial will help to identify potential benefits and limitations regarding the use of BaG in Masquelet therapy. Data from the study will increase the knowledge about BaG as a bone graft substitute as well as identify patients possibly benefiting from Masquelet therapy using BaG and those who are more likely to fail, thereby improving the quality of non-union treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pseudoarthrosis of Bone

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Masquelet technique: bioactive glass
Arm Type
Experimental
Arm Title
Masquelet technique: RIA + TCP
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
bioglass (S53P4)
Intervention Description
surgical procedure: Masquelet defect augmentation with bioglass
Intervention Type
Device
Intervention Name(s)
RIA and TCP
Intervention Description
surgical procedure: Masquelet defect augmentation with RIA and TCP
Primary Outcome Measure Information:
Title
Rate of participants with osseus consolidation evaluation via x-ray
Description
x-ray in 2 planes; union = cortical bridging of at least three out of four cortices
Time Frame
1 year post-operative Masquelet step II
Secondary Outcome Measure Information:
Title
12-item Short Form Survey (SF-12)
Description
Quality of life: Physical Score 23.99938(lowest/worst)-56.57706(highest/best), Mental Score 19.06444(lowest/worst)-60.75781 (highest/best)
Time Frame
1 year post-operative Masquelet step II
Title
Perfusion
Description
Real-time microperfusion assessment using Contrast enhanced ultra-sound (CEUS), contrasting agent: SonoVue. Objective perfusion quantification (using VueBox). Evaluation of characteristic perfusion parameters such as: wash-in rate, wash-in perfusion index
Time Frame
3 months post-operative Masquelet step II
Title
Rate of participants with osseus consolidation evaluation via CT
Description
union = cortical bridging of at least three out of four cortices
Time Frame
1 year post-operative Masquelet step II

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: pseudarthrosis of the tibia or femur bone defect < 5 cc surgical treatment with Masquelet technique Exclusion Criteria: age under 18 disagreement patients who require amputation of the affected limb
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sebastian Findeisen, Dr. med.
Phone
+4962215634330
Email
sebastian.findeisen@med.uni-heidelberg.de
First Name & Middle Initial & Last Name or Official Title & Degree
Patrick Haubruck, Dr. med.
Email
patrick.haubruck@med.uni-heidelberg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerhard Schmidmaier, Prof. Dr.
Organizational Affiliation
HTRG
Official's Role
Study Director
Facility Information:
Facility Name
University Hospital Heidelberg
City
Heidelberg
State/Province
Baden-Württemberg
ZIP/Postal Code
69118
Country
Germany
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
anonymized/pseudonymized, data that underlies results in a publication
IPD Sharing Time Frame
after conclusion and evaluation of the study
IPD Sharing Access Criteria
public
IPD Sharing URL
https://pubmed.ncbi.nlm.nih.gov/29843766/
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Evaluation of the Clinical Effectiveness of Bioactive Glass (S53P4) in the Treatment of Tibia and Femur Non-unions

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