Study Stopped
Due to local changes in patient up-take after COVID it is no longer possible to conduct the study.
Operative Versus Non-operative Treatment of Recalcitrant Plantar Fasciitis - A Randomized Study
1 other identifier
interventional
N/A
1 country
1
Brief Summary
The purpose of the study is to examine whether patients with heel spurs for more than 6 months, who have been treated conservatively, have better effect of surgery than further conservative treatment. The study is performed as a randomized trial with the inclusion of 32 patients divided between open plantar fasciectomy and conservative treatment. The primary endpoint is Self-Reported-Foot-And-Ankle Score (SEFAS-score) after 24 months. Secondary endpoints includes: Pain (Visual analogue score) at first step, rest and activity after 3, 6, 12 and 24 months, SEFAS-score after 3, 6 og 12 months, changes in gait after 6 months (measured with gait-analysis). All endpoints are measured at inclusion. The power calculation is based on the assumption that surgical treatment gives an improvement in SEFAS-score of 10 points (SD 7.9) after 24 months when compared to conservative treatment together with an alpha-value of 5 % and a beta value of 90 %.
Trial Health
Trial Health Score
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Started Jan 2022
Longer than P75 for not_applicable
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 30, 2021
CompletedFirst Posted
Study publicly available on registry
October 4, 2021
CompletedStudy Start
First participant enrolled
January 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 31, 2025
CompletedMarch 8, 2023
March 1, 2023
3.8 years
September 30, 2021
March 6, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Self-Reported-Foot-And-Ankle Score (SEFAS)
The questionnaire contains 12 items with 5 response options. The questionnaire covers different constructs, which are not reported separately in subscales. The most important of these constructs are pain, function, and limitation of function. Each of the 12 multiple-choice questions scores from 0 to 4 where a sum of 0 points represents the most severe disability and 48 represents normal function.
24 Months
Study Arms (2)
Operative treatment
EXPERIMENTALPatients treated with open plantar fasciotomy
Conservative treatment
ACTIVE COMPARATORPatients treated non-operatively with exercise
Interventions
In the surgical treated group, the plantar fascia is defined percutaneously (medial and lateral margin). An incision is then made just distal to the heel pad medially over the plantar fascia. A resection is performed 1 cm in length with a width corresponding to 50% of the medial band. The skin is sutured with nylon/nonresorbable suture. Postoperatively, the operated foot is elevated for the first 24 hours. Then free mobilization in postoperative shoe (ProCare shoe) is allowed. The dressing is left untouched for 3-5 days, after which it can be changed to a patch. After 14 days the sutures are removed and the patient allowed using regular shoes.
In the conservative treatment group, patients are instructed in performing stretching exercises with plantar fascia specific stretching exercises 10 x 10 seconds, 3 times daily and high load strength training are every other day for 3 months. Each high load strength exercise consists of 3 seconds of concentric phase (lifting up with the heel) and 3 seconds of eccentric phase (lowering the heel) with 2 seconds of isometric pause (pause at maximum lifted heel). 12 repetitions max (RM) are performed, defined as the maximum (over) weight the patient can lift 12 times with full range of motion while performing the exercise correctly. 3 x 12 exercises are performed per workout. After 2 weeks, the load is while the number of repetitions is reduced to 10 RM with an increase to 4 repetitions per workout. After 4 weeks the intensity is increased to 8RM with 5 set. Patients are instructed to increase the load throughout the training period.
Eligibility Criteria
You may qualify if:
- Age \> 18 years.
- Isolated plantar fasciitis through more than 6 months
- Ultrasonic verification of diagnosis (plantar fascia \>4 mm)
- Ability to follow the post-operative- and conservative plans
- Able to give informed consent.
You may not qualify if:
- Previous surgical treatment of plantar fasciitis or surgery around the heel
- Rheumatic disease
- Diabetes
- Dementia
- Neuropathy
- Known alcohol abuse
- Pareses/paralysis of the affected extremity.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hvidovre Hospital, Department of Ortopedic Surgery
Hvidovre, 2300, Denmark
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD., Principal Investigator
Study Record Dates
First Submitted
September 30, 2021
First Posted
October 4, 2021
Study Start
January 1, 2022
Primary Completion
October 31, 2025
Study Completion
October 31, 2025
Last Updated
March 8, 2023
Record last verified: 2023-03
Data Sharing
- IPD Sharing
- Will not share