Medial Displacement Calcaneal Osteotomy and FDL- Transfer - With a Human, Allogeneic Cortical Bone Screw
Recruiting
Observational Study
Flat Feet
Flexor Tendon Rupture
Tibialis Posterior Dysfunction
Deformity, Foot
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 40 (estimated)
- Sponsor
- Orthopedic Hospital Vienna Speising · Other
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
The goal of this observational study is to compare the use of a screw made of human bone (Shark-Screw®, Surgebright-GmbH) with the metal/Bio-Tenodesis screw (Arthrex) in the treatment of the symptomatic flatfoot using the medializing calcaneus osteotomy with flexor digitorum longus transfer (FDL) in adult patients. The advantage of the human bone screw is that after surgery no hardware removal is …
Trial Locations
Loading…
Loading trial locations…
Eligibility Criteria
Inclusion Criteria
* Indication for the use of a metal/Bio-Tenodesis screw or human bone screw in medializing calcaneus osteotomy with FDL transfer.
* BMI\< 40 kg/m²
Exclusion Criteria:
* Insufficient knowledge of German
* Alcohol and drug abuse
* Pregnant woman or nursing mother
* Foreseeable co…
Contacts