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Operative Versus Non-operative Treatment of Recalcitrant Plantar Fasciitis - A Randomized Study

Primary Purpose

Plantar Fascitis, Surgical Treatment, Non-operative Treatment

Status
Withdrawn
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Open plantar fasciotomy
Conservative treatment
Sponsored by
Hvidovre University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Plantar Fascitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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.

Sites / Locations

  • Hvidovre Hospital, Department of Ortopedic Surgery

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Operative treatment

Conservative treatment

Arm Description

Patients treated with open plantar fasciotomy

Patients treated non-operatively with exercise

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Full Information

First Posted
September 30, 2021
Last Updated
March 6, 2023
Sponsor
Hvidovre University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05066919
Brief Title
Operative Versus Non-operative Treatment of Recalcitrant Plantar Fasciitis - A Randomized Study
Official Title
Operative Versus Non-operative Treatment of Recalcitrant Plantar Fasciitis - A Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Due to local changes in patient up-take after COVID it is no longer possible to conduct the study.
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
October 31, 2025 (Anticipated)
Study Completion Date
October 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital

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
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 %.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plantar Fascitis, Surgical Treatment, Non-operative Treatment, Randomized Study

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Operative treatment
Arm Type
Experimental
Arm Description
Patients treated with open plantar fasciotomy
Arm Title
Conservative treatment
Arm Type
Active Comparator
Arm Description
Patients treated non-operatively with exercise
Intervention Type
Procedure
Intervention Name(s)
Open plantar fasciotomy
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Conservative treatment
Intervention Description
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.
Primary Outcome Measure Information:
Title
Self-Reported-Foot-And-Ankle Score (SEFAS)
Description
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.
Time Frame
24 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: 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.
Facility Information:
Facility Name
Hvidovre Hospital, Department of Ortopedic Surgery
City
Hvidovre
ZIP/Postal Code
2300
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Operative Versus Non-operative Treatment of Recalcitrant Plantar Fasciitis - A Randomized Study

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