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A Study to Compare Early and Partial Weight-bearing After Hallux Valgus Surgery

Primary Purpose

Hallux Valgus, Orthopedic Disorder

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Partial weight-bearing (10 - 15kg)
Complete weight-bearing
Sponsored by
Ente Ospedaliero Cantonale, Bellinzona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hallux Valgus focused on measuring Quality of life, Bone consolidation, Foot surgery, Lapidus surgery, Weil surgery, Hohmann surgery, Akin surgery

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patient who undergo modified Lapidus arthrodesis operation and associated with:
  • Additional surgical gestures such as e.g. interventions on the proximal phalanx of the first finger (Akin) or interventions on the 2nd and / or 3rd ray (Weil / Hohmann) [23,24].
  • Willingness and ability to participate in the trial
  • Signed Informed Consent

Exclusion Criteria:

  • Diabetes mellitus
  • Rheumatoid arthritis
  • Previous foot surgery
  • Classic Lapidus surgery
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, general physical problem of the participant, etc.
  • Inability or contraindications to undergo the investigated intervention
  • Pregnant women

Sites / Locations

  • EOCRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Partial weight-bearing (10 - 15kg)

Complete weight-bearing

Arm Description

Immediate post-operative partial weight-bearing (10 - 15kg) with a VACOPASO shoe for 6 weeks, crutches and antithrombotic prophylaxis

Immediate post-operative complete weight-bearing with a VACOPASO shoe for 6 weeks and antithrombotic prophylaxis

Outcomes

Primary Outcome Measures

Subjective functional recovery measured by Olerud and Molander Ankle Score (OMAS)
The Olerud and Molander Ankle Score (OMAS) is a functional rating scale from 0 to 100 and is based on nine different items: pain, stiffness, swelling, stair climbing, running, jumping, squatting, supports and activities of daily living. Higher scores mean a better outcome.

Secondary Outcome Measures

Pain on a Visual Analogue Scale
Change in pain severity postoperatively measured using the pain Visual Analogue Scale (VAS). The pain VAS scale is a validated, self-assessment scale in which patients rate their pain by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" (0) and "worst pain" (10).
Bone consolidation through anteroposterior and lateral foot x-rays
Incidence of bone consolidation (bone callus formation) assessed in an objective measure by the radiologist
American Orthopedic Foot and Ankle Score questionnaire
The American Orthopedic Foot and Ankle Score (AOFAS) is used find the quality of life index for foot-and-ankle pathologies. It is made of nine questions and cover three categories: Pain (40 points), function (50 points) and alignment (10 points). These are all scored together for a total of 100 points. Higher scores mean a better outcome.
Subjective functional recovery measured by Olerud and Molander Ankle Score (OMAS)
Subjective functional recovery through the Olerud and Molander Ankle Score (OMAS). The Olerud and Molander Ankle Score (OMAS) [7] is a functional rating scale from 0 to 100 and is based on nine different items: pain, stiffness, swelling, stair climbing, running, jumping, squatting, supports and activities of daily living. Higher scores mean a better outcome.

Full Information

First Posted
September 6, 2022
Last Updated
April 21, 2023
Sponsor
Ente Ospedaliero Cantonale, Bellinzona
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1. Study Identification

Unique Protocol Identification Number
NCT05534724
Brief Title
A Study to Compare Early and Partial Weight-bearing After Hallux Valgus Surgery
Official Title
Is Full Weight Bearing After the Modified Lapidus Operation Possible? A Randomized Controlled Trial to Compare Early and Partial Weight-bearing
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 19, 2023 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
January 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ente Ospedaliero Cantonale, Bellinzona

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a two-arm randomized controlled trial with the aim to evaluate the effectiveness and safety of post-operative management after a modified Lapidus arthrodesis with/without an Akin or a Weil/Hohmann surgery fusion with immediate complete weight-bearing compared with partial weight-bearing (10 - 15kg) for 6 weeks as a novel approach for rehabilitation after a foot surgery.
Detailed Description
The surgical operation will be carried out according to the standard clinical practice, namely following the modified Lapidus general and specific rules concerning the surgical treatment of hallux valgus with/without an Akin or a Weil/Hohmann surgery fusion. Post-operatively, patients who meet the eligibility criteria will be randomized into one of the two groups (partial weight-bearing limited at 15kg vs full weight-bearing) Patient in both groups will be wearing a VACOPASO shoe for 6 weeks. Standard X-ray assessment to determine healing, hardware fixation, fracture alignment, fracture reduction, implants mobilization will be performed at weeks 6, 12, 24. Change in pain severity from the day of surgery to 6, 12 and 24 weeks postoperatively will be measured using the pain Visual Analogue Scale (VAS). Quality of life will be assessed through the American Orthopedic Foot and Ankle Score (AOFAS). Subjective functional recovery through the Olerud and Molander Ankle Score (OMAS).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hallux Valgus, Orthopedic Disorder
Keywords
Quality of life, Bone consolidation, Foot surgery, Lapidus surgery, Weil surgery, Hohmann surgery, Akin surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The surgical operation will be the modified Lapidus arthrodesis of hallux valgus with/without an Akin or a Weil/Hohmann surgery fusion. Post-operatively, patients will be randomized into one of the two groups: Group A (control intervention): immediate post-operative partial weight-bearing (10 - 15kg) with a VACOPASO for 6 weeks, crutches and antithrombotic prophylaxis. Group B (experimental intervention): immediate post-operative complete weight-bearing with a VACOPASO for 6 weeks and antithrombotic prophylaxis.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
122 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Partial weight-bearing (10 - 15kg)
Arm Type
Other
Arm Description
Immediate post-operative partial weight-bearing (10 - 15kg) with a VACOPASO shoe for 6 weeks, crutches and antithrombotic prophylaxis
Arm Title
Complete weight-bearing
Arm Type
Experimental
Arm Description
Immediate post-operative complete weight-bearing with a VACOPASO shoe for 6 weeks and antithrombotic prophylaxis
Intervention Type
Other
Intervention Name(s)
Partial weight-bearing (10 - 15kg)
Intervention Description
Immediate post-operative partial weight-bearing (10 - 15kg) with a VACOPASO shoe for 6 weeks
Intervention Type
Other
Intervention Name(s)
Complete weight-bearing
Intervention Description
Complete post-operative weight-bearing with a VACOPASO shoe for 6 weeks
Primary Outcome Measure Information:
Title
Subjective functional recovery measured by Olerud and Molander Ankle Score (OMAS)
Description
The Olerud and Molander Ankle Score (OMAS) is a functional rating scale from 0 to 100 and is based on nine different items: pain, stiffness, swelling, stair climbing, running, jumping, squatting, supports and activities of daily living. Higher scores mean a better outcome.
Time Frame
at 6 weeks
Secondary Outcome Measure Information:
Title
Pain on a Visual Analogue Scale
Description
Change in pain severity postoperatively measured using the pain Visual Analogue Scale (VAS). The pain VAS scale is a validated, self-assessment scale in which patients rate their pain by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" (0) and "worst pain" (10).
Time Frame
At the day of surgery, at 6, 12 and 24 weeks postoperatively.
Title
Bone consolidation through anteroposterior and lateral foot x-rays
Description
Incidence of bone consolidation (bone callus formation) assessed in an objective measure by the radiologist
Time Frame
6 weeks and 12 weeks. At 24 weeks in case of fracture non-union reported at the 12th week postoperatively
Title
American Orthopedic Foot and Ankle Score questionnaire
Description
The American Orthopedic Foot and Ankle Score (AOFAS) is used find the quality of life index for foot-and-ankle pathologies. It is made of nine questions and cover three categories: Pain (40 points), function (50 points) and alignment (10 points). These are all scored together for a total of 100 points. Higher scores mean a better outcome.
Time Frame
at 6, 12 and 24 weeks
Title
Subjective functional recovery measured by Olerud and Molander Ankle Score (OMAS)
Description
Subjective functional recovery through the Olerud and Molander Ankle Score (OMAS). The Olerud and Molander Ankle Score (OMAS) [7] is a functional rating scale from 0 to 100 and is based on nine different items: pain, stiffness, swelling, stair climbing, running, jumping, squatting, supports and activities of daily living. Higher scores mean a better outcome.
Time Frame
at 12 and 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patient who undergo modified Lapidus arthrodesis operation and associated with: Additional surgical gestures such as e.g. interventions on the proximal phalanx of the first finger (Akin) or interventions on the 2nd and / or 3rd ray (Weil / Hohmann) [23,24]. Willingness and ability to participate in the trial Signed Informed Consent Exclusion Criteria: Diabetes mellitus Rheumatoid arthritis Previous foot surgery Classic Lapidus surgery Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, general physical problem of the participant, etc. Inability or contraindications to undergo the investigated intervention Pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Martin Riegger, MD
Phone
0041918117029
Email
RicercaOrtopedia.ORL@eoc.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin Riegger, MD
Organizational Affiliation
EOC
Official's Role
Principal Investigator
Facility Information:
Facility Name
EOC
City
Lugano
ZIP/Postal Code
6900
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Martin Riegger, Dr.med
Phone
+41 (0) 91 811 70 29
Email
RicercaOrtopedia.ORL@eoc.ch

12. IPD Sharing Statement

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Citation
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Links:
URL
http://oped.ch/vacopaso-free
Description
VACOpaso Free OPED

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A Study to Compare Early and Partial Weight-bearing After Hallux Valgus Surgery

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