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

Sponsor
Sebastian Findeisen (Other)
Overall Status
Recruiting
CT.gov ID
NCT05049915
Collaborator
Bonalive Biomaterials Ltd (Industry)
50
1
2
55
0.9

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Device: bioglass (S53P4)
  • Device: RIA and TCP
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
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
Actual Study Start Date :
Jun 1, 2018
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Masquelet technique: bioactive glass

Device: bioglass (S53P4)
surgical procedure: Masquelet defect augmentation with bioglass

Active Comparator: Masquelet technique: RIA + TCP

Device: RIA and TCP
surgical procedure: Masquelet defect augmentation with RIA and TCP

Outcome Measures

Primary Outcome Measures

  1. Rate of participants with osseus consolidation evaluation via x-ray [1 year post-operative Masquelet step II]

    x-ray in 2 planes; union = cortical bridging of at least three out of four cortices

Secondary Outcome Measures

  1. 12-item Short Form Survey (SF-12) [1 year post-operative Masquelet step II]

    Quality of life: Physical Score 23.99938(lowest/worst)-56.57706(highest/best), Mental Score 19.06444(lowest/worst)-60.75781 (highest/best)

  2. Perfusion [3 months post-operative Masquelet step II]

    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

  3. Rate of participants with osseus consolidation evaluation via CT [1 year post-operative Masquelet step II]

    union = cortical bridging of at least three out of four cortices

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Heidelberg Heidelberg Baden-Württemberg Germany 69118

Sponsors and Collaborators

  • Sebastian Findeisen
  • Bonalive Biomaterials Ltd

Investigators

  • Study Director: Gerhard Schmidmaier, Prof. Dr., HTRG

Study Documents (Full-Text)

More Information

Publications

Responsible Party:
Sebastian Findeisen, Intern, University Hospital Heidelberg
ClinicalTrials.gov Identifier:
NCT05049915
Other Study ID Numbers:
  • S-472/2017
First Posted:
Sep 20, 2021
Last Update Posted:
Sep 20, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 20, 2021