- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04823884
Short-term Results After Minimally Invasive Chevron Osteotomy for Hallux Valgus Correction
Short-term Results After Minimally Invasive Chevron Osteotomy for Hallux Valgus Correction in Comparison to the Open Technique
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Tyrol
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Innsbruck, Tyrol, Austria, 6020
- Priv-Doz. Dr. Gerhard Kaufmann
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- all patients undergoing hallux valgus correction by means of a distal chevron osteotomy
Exclusion Criteria:
- surgery on the lesser rays of the same foot
- mental illness with impossibility to follow the postoperative protocol
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: open distal chevron osteotomy
Hallux valgus correction is provided by using the traditional open distal v-shaped chevron osteotomy.
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Through a 4-cm-long dorsomedial skin incision the V-shaped osteotomy with the apex 1-2 mm superior to the center of the metatarsal head is performed.
The angle of the chevron is 60° to 90°.
The direction of the osteotomy is angled toward the center of the third metatarsal head.
After shifting the metatarsal head laterally, fixation is achieved by usage of one cannulated screw (3.0 mm or 2.5mm).
Prominent bone ridges are resected with a saw.
A distal soft tissue procedure is performed in every case through the same skin incision.
The adductor hallucis tendon is detached from its insertion at the phalangeal bone and from the lateral border of the fibular sesamoid.
The transverse intermetatarsal ligament is released and a T-shaped capsulotomy is performed to allow reposition of the sesamoids.
Sesamoid position is controlled by sight.
After closing of the medial capsula skin is closed with nylon sutures.
Other Names:
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Active Comparator: minimally invasive distal chevron osteotomy
Hallux valgus correction is provided by using a minimally invasive distal v-shaped chevron osteotomy.
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The osteotomy is performed percutaneously through a dorsomedial incision of 3-5 mm.
An electric motor-driven machine used for the osteotomy.
To prevent overheating the reamer is frequently rinsed with sterile saline.
The medial eminence is excised and the V-shaped osteotomy is performed.
The apex of the osteotomy is identified by fluoroscopy and centered 1-2 mm superior to the center of the metatarsal head.
The angle of the osteotomy amounts to 60-90 degrees as well.
Bone debris is washed out with sterile saline.
A lateral soft-tissue release is undertaken through a separate lateral incision of 3-5 mm.
The distal fragment is shifted laterally and fixed with a canulated screw of 3.5mm.
Residual bone ridges are reamed.
Position of the metatarsal head and the K-wire is controlled by fluoroscopy.
The skin is closed with a nylon sutures.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: Change of the scores from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome is assessed for both techniques with a clinical score to specific time points. Maryland Foot Score [maximum 100 points, minimum 0 points - higher scores mean better outcome] |
Change of the scores from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: Change of the SF 12 score from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical general situation is assessed for both techniques to specific time points by using the SF12 Life Quality Score [maximum 47 points, minimum 0 points - higher scores mean better clinical situation]
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Change of the SF 12 score from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: Change of the VAS from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome and therefore the pain level is assessed for both techniques to specific time points by using the Visual Analogue Score for pain [0-10])
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Change of the VAS from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: Change of the range of motion and therefore the clinical outcome from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome is assessed for both techniques to specific time points by assessing the Range of motion (normal range 70-0-45 degrees)
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Change of the range of motion and therefore the clinical outcome from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: Change of the foot circumference at the level of surgery from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome and therefore changes of the foot circumference at the level of surgery is assessed for both techniques to specific time points by measuring the foot circumference at the level of surgery (measurement in centimeter).
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Change of the foot circumference at the level of surgery from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
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Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: Change of the scores from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
|
Clinical outcome is assessed for both techniques with a clinical score to specific time points. AOFAS Hallux etmatarsophalangeal -interphalangeal Scale [maximum 100 points, minimum 0 points - higher scores mean better outcome] |
Change of the scores from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
|
|
Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: Change of the score from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
|
Clinical outcome is assessed for both techniques with clinical a score to specific time points. JSSF Hallux metatarsophalangeal -interphalangeal Scale [maximum 100 points, minimum 0 points - higher scores means better outcome] |
Change of the score from preoperative to postoperative at 2 weeks, 4 weeks, 6 and 12 weeks is measured
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical outcome after correction of hallux valgus deformity within the first three months after surgery: a comparison of the minimally invasive versus the open distal chevron osteotomy technique .
Time Frame: This score is used to compare the clinical fitness of both cohorts preoperatively.
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Clinical fitness of our cohort is assessed by means of the Charlson Comorbidity Index [maximum 37 points, minimum 0 points - lower scores mean clinical situation] preoperatively.
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This score is used to compare the clinical fitness of both cohorts preoperatively.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021/1000
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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