A Comparative Trial of a Minimal-invasive Technique Versus Open Arthrodesis in the Treatment of Midfoot Arthritis
Primary Purpose
Osteoarthritis, Foot, Osteotomy
Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
reverse distal metatarsal minimal-invasive osteotomy
tarsometatarsal fusion
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis
Eligibility Criteria
Inclusion Criteria:
- Patients older than 18 years
- Midfoot arthritis of lesser TMTJ (second, third, rarely fourth and fifth) with ongoing disabling pain
- Able to give informed consent as documented by signature
- failed conservative treatment for a period of at least 3 months (CSI injections and/or orthotic devices)
Exclusion Criteria:
- Concomitant fusion of 1st TMTJ
- Patients younger than 18 years
- Contraindication to undergo surgery or general anaesthesia
- Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.
- pregnancy
Sites / Locations
- Kantonsspital BadenRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Group A
Group B
Arm Description
Patients suffering from midfoot arthritis after failed prior conservative therapy who undergo a reverse distal metatarsal minimal-invasive osteotomy
Patients suffering from midfoot arthritis after failed prior conservative therapy who undergo a fusion of one or more midfoot (tarsometatarsal) joints
Outcomes
Primary Outcome Measures
Clinical Outcome using a patient related outcome measure, the FAAM score (Validated Foot and Ankle Ability Measure). The score is a self-report outcome instrument developed to assess physical function. The change between the time points is measured.
FAAM score, the highest score is 100, indicating the best possible outcome
Secondary Outcome Measures
Duration of procedure
Duration of procedure (in minutes from first incision until wound is closed)
Length of hospital stay
Length of hospital stay in days
Visual Analogue Scale (VAS) score. It is a measurement instrument for the amount of pain that a patient feels. The score is assessed preoperatively and the change between the time points is measured.
Pain score (scale 0-10, where 10 is the maximum pain)
Radiological union by evaluating conventional X-Ray. Preoperative X-Rays and postoperative X-Rays are comparted and the change in union in terms of bone densitiy is assessed postoperatively.
Union of bone on conventional X-Ray in two planes (dorsoplantar and lateral views)
Complications
Identifying minor and major complications of the procedure (e.g. infections)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04894578
Brief Title
A Comparative Trial of a Minimal-invasive Technique Versus Open Arthrodesis in the Treatment of Midfoot Arthritis
Official Title
Can Reverse Oblique Distal Minimal-invasive Osteotomies Replace Arthrodesis of the Tarsometatarsal Joints? - a Prospective, Comparative Trial of 50 Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Recruiting
Study Start Date
May 14, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kantonsspital Baden
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Group A: Patients suffering from midfoot arthritis after failed prior conservative therapy who undergo a reverse distal metatarsal minimal-invasive osteotomy Group B: Patients suffering from midfoot arthritis after failed prior conservative therapy who undergo a fusion of one or more midfoot (tarsometatarsal) joints
Detailed Description
Midfoot arthritis is a common condition leading to disabling chronic foot pain that affects activities of daily living. The causes can be primary osteoarthritis (OA), inflammatory or post-traumatic. We are looking at OA of the lesser (second and/or third) tarsometatarasal joints (TMTJ). Orthotics, customised shoes or steroid injections are options to treat this condition nonoperatively. If these measures fail, arthrodesis of the arthritic joints represents the standard procedure to surgical treatment. Generally, the results of this procedure are at a satisfactory level for the patients, nevertheless, there is a relevant amount of patients with residual pain, lack of a normal foot appearance, and the need for unplanned surgery or use of orthotics postoperatively. Furthermore, patients undergoing an arthrodesis of the lesser TMTJ usually have to stay in hospital for 4-7 days. Postoperatively, patients are only allowed to partially weightbear for at least 6 weeks and need a cast for six weeks as well. During that time thrombosis prophylaxis is administered for about 6 weeks.
The conventional distal minimal-invasive metatarsal osteotomy (DMMO) is an accepted technique for metatarsal osteotomies. Recently, Schneider et al. presented results of a modification of the conventional DMMO, the reverse DMMO to treat OA of the lesser TMTJ, thus representing an alternative treatment to arthrodesis. The procedure has many benefits. It allows outpatient care, an immobilisation in a cast is not necessary. Instead, patients have to wear a flat postoperative shoe for 2-3 weeks and are allowed to fully weightbear from day one after surgery. Therefore, thrombosis prophylaxis is not necessary unless there are specific risk factors.
However, while the arthrodesis directly addresses the arthritic joints, the R-DMMO alters the ground reaction force of the metatarsal head leading to less stress at the level of the TMTJ, but the arthritic joint itself is not approached. Still, the results presented by Schneider et al. are promising. Since there was no group to compare the treatment with, the small sample size, and a retrospective design, we would like to prospectively compare these two surgical procedures directly in order to find out whether or not the R-DMMO can be recommended as a standard procedure for OA of the lesser TMTJ at a much more convenient level for patients regarding the whole perioperative protocol. No vulnerable population is included. The scientific value is remarkable since this would be the first study to examine this matter and we are able to provide a high level of evidence due to the prospective-randomised and comparative design of the study. All legal requirements will be fulfilled and the ethical standards are guaranteed.
Both procedures have been described and the technique of the DMMO itself is not new, but its modification (R-DMMO) represents a new approach for this condition. Both procedures are reliable and safe, which is why the risk category of the study is A according to ClinO, Art. 61.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Foot, Osteotomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group A
Arm Type
Active Comparator
Arm Description
Patients suffering from midfoot arthritis after failed prior conservative therapy who undergo a reverse distal metatarsal minimal-invasive osteotomy
Arm Title
Group B
Arm Type
Active Comparator
Arm Description
Patients suffering from midfoot arthritis after failed prior conservative therapy who undergo a fusion of one or more midfoot (tarsometatarsal) joints
Intervention Type
Procedure
Intervention Name(s)
reverse distal metatarsal minimal-invasive osteotomy
Intervention Description
minimal-invasive oblique osteotomy of the two or three metatarsal bones using a straight burr
Intervention Type
Procedure
Intervention Name(s)
tarsometatarsal fusion
Intervention Description
open procedure with fusion and screw and plate fixation of two to three tarsometatarsal joints
Primary Outcome Measure Information:
Title
Clinical Outcome using a patient related outcome measure, the FAAM score (Validated Foot and Ankle Ability Measure). The score is a self-report outcome instrument developed to assess physical function. The change between the time points is measured.
Description
FAAM score, the highest score is 100, indicating the best possible outcome
Time Frame
6 weeks, 3 months, 6 months, 12 and 24 months post surgery
Secondary Outcome Measure Information:
Title
Duration of procedure
Description
Duration of procedure (in minutes from first incision until wound is closed)
Time Frame
through study completion, an average of 2 years
Title
Length of hospital stay
Description
Length of hospital stay in days
Time Frame
through study completion, an average of 2 years
Title
Visual Analogue Scale (VAS) score. It is a measurement instrument for the amount of pain that a patient feels. The score is assessed preoperatively and the change between the time points is measured.
Description
Pain score (scale 0-10, where 10 is the maximum pain)
Time Frame
6 weeks, 3 months, 6 months, 12 and 24 months post surgery
Title
Radiological union by evaluating conventional X-Ray. Preoperative X-Rays and postoperative X-Rays are comparted and the change in union in terms of bone densitiy is assessed postoperatively.
Description
Union of bone on conventional X-Ray in two planes (dorsoplantar and lateral views)
Time Frame
6 weeks, 3 months, 6 months, 12 and 24 months post surgery
Title
Complications
Description
Identifying minor and major complications of the procedure (e.g. infections)
Time Frame
6 weeks, 3 months, 6 months, 12 and 24 months post surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients older than 18 years
Midfoot arthritis of lesser TMTJ (second, third, rarely fourth and fifth) with ongoing disabling pain
Able to give informed consent as documented by signature
failed conservative treatment for a period of at least 3 months (CSI injections and/or orthotic devices)
Exclusion Criteria:
Concomitant fusion of 1st TMTJ
Patients younger than 18 years
Contraindication to undergo surgery or general anaesthesia
Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.
pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Karim Eid, PD Dr. med.
Phone
0564863062
Email
karim.eid@ksb.ch
Facility Information:
Facility Name
Kantonsspital Baden
City
Baden
State/Province
Aargau
ZIP/Postal Code
5400
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karim Eid, PD Dr. med.
Phone
0041564862888
Email
karim.eid@ksb.ch
First Name & Middle Initial & Last Name & Degree
Christopher G Lenz, Dr. med.
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
26869495
Citation
Gougoulias N, Lampridis V. Midfoot arthrodesis. Foot Ankle Surg. 2016 Mar;22(1):17-25. doi: 10.1016/j.fas.2015.04.004. Epub 2015 Apr 24.
Results Reference
background
PubMed Identifier
31653366
Citation
Laffenetre O, Perera A. Distal Minimally Invasive Metatarsal Osteotomy ("DMMO" Procedure). Foot Ankle Clin. 2019 Dec;24(4):615-625. doi: 10.1016/j.fcl.2019.08.011.
Results Reference
background
PubMed Identifier
32086136
Citation
Schneider TE, Varrall CR, Malhotra K. Early results of minimally invasive, reverse-oblique, distal metaphyseal metatarsal osteotomy (R-DMMO) for arthritis of the lesser tarsometatarsal joints - A retrospective case series. Foot (Edinb). 2020 Jun;43:101652. doi: 10.1016/j.foot.2019.10.007. Epub 2019 Oct 25.
Results Reference
background
Learn more about this trial
A Comparative Trial of a Minimal-invasive Technique Versus Open Arthrodesis in the Treatment of Midfoot Arthritis
We'll reach out to this number within 24 hrs