Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT06211504 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Sinus Tarsi Implant as an Adjuvant Procedure to Medial Displacement Calcaneal Osteotomy in the Treatment of Mobile Adult Acquired Flatfoot Deformity

StatusRecruiting
PhasePhase 4
Started2024-07-31
View on ClinicalTrials.gov ↗

Amendment history

2025-11-24
minor
Study Status v5
Primary completion date2026-07-31→2027-12-31
Completion date2028-07-31→2029-12-31
2025-10-07
minor
Study Status, Study Description, Eligibility, Contacts/Locations v4
Study sites9→10
Eligibility criteria+96 characters
Inclusion Criteria: Patients with AAFD stage IIAII, within whom the talonavicular uncoverage is not exceedingconsidered 40%by the treating surgeon to require an additional lateral column lengthening Age 16-75 years, either sex Failed non-surgical treatment i [...]
Study description+33 characters
[...] ne University Hospital in Malmö, Capio Ortho Center in Malmö and Göteborg, Sahlgrenska University hospital in Mölndal, Uppsala Univer [...] tcome measures Changes in the alignment of the foot will be assessedoutassessed with weight-bearing radiographs measuring specific angles a [...] l by the Swedish Ethical Review Authority (Dnr 2023-02892-01 and DNR 2025-05078-02). Recruitment strategy and timeline The 910 included orthopedic centers involved in this trail have an [...]
2024-11-14
minor
Study Status v3
Primary completion date2026-07-08→2026-07-31
Completion date2028-07-08→2028-07-31
Start dateestimated 2024-07-08→confirmed 2024-07-31
2024-07-03
minor
Study Status, Study Description v2
Primary completion date2026-04-11→2026-07-08
Completion date2028-04-11→2028-07-08
Start date2024-04-11→2024-07-08
Study description+1 characters
[...] in accordance with the declaration of Helsinki. The project willhas bebeen examined and received approval by the Swedish Ethical Review Authority before(Dnr any part of the trial is initiated2023-02892-01). Recruitment strategy and timeline The 9 included orthopedi [...]
2024-04-12
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2026-02-01→2026-04-11
Completion date2027-02-01→2028-04-11
Start date2024-02-01→2024-04-11
Study sitesdetails revised at 9 of 9 sites
2024-01-08
minor
Original filing
146 trials monitored
See 5 trials at risk
Background: Adult acquired flatfoot deformity (AAFD) is a deformity of the foot which leads to pain and an altered gait pattern. There are several different surgical interventions available for treatment of AAFD. One of the most common treatments for mobile AAFD is medial displacement calcaneal osteotomy (MDCO) with or without adjuvant soft tissue procedures. However, the medial displacement of the calcaneus only aims to correct the deformity in one plane despite AAFD being a deformity of three planes with hypereversion of the calcaneus, anterior translation of the talus over the calcaneus and tilting/drop of the calcaneal head. Because of these multiple forces, the healing of MDCO in the intended position can sometimes be hard to achieve and medial soft tissue is still stressed leading to recurring deformity. The investigators believe that adjuvant insertion of a sinus tarsi implant (STI) could work as an internal splint, protecting soft tissue procedures on the medial side, reversing anterior translation of the talus, opposing calcaneus eversion, and lifting talar head. This additional procedure will create a better correction of the deformity with enhanced appearance of the foot and better long-term functional results. Methods: This is a multi-center randomized controlled trial designed to assess the efficacy of STI as an adjuvant procedure to MDCO in patients with mobile AAFD (Stage II). Patients aged 16 to 75 years, referred to one of the orthopedic centers involved in this study, will be invited to participate if they fulfil the trials eligibility criteria. In total, 130 patients who provide informed consent will be randomized to either MDCO with STI or MDCO without STI (65 patients in each group). The included patients will be clinically and radiographically examined. They will also fill out a form before surgery and 4-5 months, 1 year and 2 years postoperatively. The form will include Self-Reported Foot and Ankle Score (SEFAS) and Euro-QoL 5 Dimensions (EQ-5D). The trials primary outcome will be change in Meary's angle. Secondary outcomes include additional radiographic changes, change in SEFAS score, EQ-5D index, pain according to visual analog scale (VAS), satisfaction assessment, clinical outcome measures, the length of postoperative sick-leave and rate of complications. Discussion: This is the first randomized controlled trial assessing the efficacy of a sinus tarsi implant as an adjuvant procedure to MDCO.
Trial Details
NCT Number NCT06211504
Lead Sponsor Region Skane
Conditions Acquired Adult Flatfoot Deformity, Flat Foot, Flexible Flatfoot
Enrollment 130 participants
Start Date 2024-07-31
Primary Completion 2027-12-31 (estimated)
Study Completion 2029-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-12-02