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

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Procedure, Device
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 16
Maximum Age: 75
Healthy Volunteers: f
View:

• Patients with AAFD stage II, in whom the talonavicular uncoverage is not considered by the treating surgeon to require an additional lateral column lengthening

• Age 16-75 years, either sex

• Failed non-surgical treatment including 3 months of physiotherapy

Locations
Other Locations
Sweden
Department of Orthopedics - Eksjö Hospital
NOT_YET_RECRUITING
Eksjö
Department of Orthopedics - Falun Hospital
NOT_YET_RECRUITING
Falun
Capio Ortho Center Göteborg
RECRUITING
Gothenburg
Department of Orthopedics - Hässleholm Hospital
RECRUITING
Hässleholm
Capio Ortho Center
RECRUITING
Malmo
Department of Orthopedics - Skåne University Hospital Malmö
NOT_YET_RECRUITING
Malmo
Department of Orthopedics - Sahlgrenska University Hospital
NOT_YET_RECRUITING
Mölndal
Department of Orthopedics - Östersund Hospital
RECRUITING
Östersund
Department of Orthopedics - Uppsala University Hospital
RECRUITING
Uppsala
Department of Orthopedics - Växjö
NOT_YET_RECRUITING
Vaxjo
Contact Information
Primary
Ida Osbeck, MD
ida.osbeck@skane.se
+46 708 49 73 79
Backup
Isam Atroshi, MD, PhD
isam.atroshi@skane.se
+46 44 309 12 60
Time Frame
Start Date: 2024-07-31
Estimated Completion Date: 2028-07-31
Participants
Target number of participants: 130
Treatments
Active_comparator: MDCO without STI
1. For patients with preoperative gastrocnemius-soleus complex tightness, defined as a preoperative dorsal extension of the ankle less than 5 degrees, with the knee completely extended, a Strayer´s procedure will be performed before the other procedures.~2. MDCO will be performed where the distal aspect of the calcaneus is separated from the proximal aspects, slided medially and fixed with two screws.~3. After the MDCO, FDL will be transferred to the navicular bone.~4. The spring ligament will be assessed. If ruptured, it will be reconstructed. If not ruptured, it will be tightened.~5. A plantarflexing open wedge osteotomy of the medial cuneiform (Cotton osteotomy) will be performed if pre-/perioperative findings indicate it.
Experimental: MDCO with STI
1. In patients with preoperative gastrocnemius-soleus complex tightness, defined as a preoperative dorsal extension of the ankle less than 5 degrees, with the knee completely extended, a Strayer´s procedure will be performed before the other procedures.~2. Thereafter, an STI (ProStop® Arthroereisis Subtalar Implant, Arthrex GmbH, Munich, Germany) will be inserted into the sinus tarsi.~3. MDCO will be performed where the distal aspect of the calcaneus is separated from the proximal aspects, slided medially and fixed with two screws.~4. After the MDCO, FDL will be transferred to the navicular bone.~5. The spring ligament will be assessed. If ruptured, it will be reconstructed. If not ruptured, it will be tightened.~6. A plantarflexing open wedge osteotomy of the medial cuneiform (Cotton osteotomy) will be performed if pre-/perioperative findings indicate it.
Related Therapeutic Areas
Sponsors
Leads: Region Skane

This content was sourced from clinicaltrials.gov