Proximal Medial Gastriocnemius Recession for Chronic Plantar Fasciitis

Chronic Plantar Fasciitis Clinical Trial

Official title:

Proximal Medial Gastriocnemius Recession for Chronic Plantar Fasciitis - a Prospective Kohort Study

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05162144
• Other study ID #: REK317597
• Status: Active, not recruiting
• Phase: N/A
• Start date: December 15, 2021
• Est. completion date: March 15, 2026

Study information

• Verified date: April 2024
• Source: Ostfold Hospital Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This prospective kohort study will follow 150 patients treated with proximal medial gastrocnemius recession for plantar fasciitts. Follow up time is two years and the main outcome is the Manchester Oxford Foot Questionnaire. A regression analasys will be performed to identify possible patient baseline factors that may affect the effect of surgery,

Description:

Recent studies indicate that chronic plantar fasciitis can be treated effectively with Proximal Medial Gastrocnemius Recession (PMGR). In our hospital this treatment has been inocorporated into routine care. This prospective kohort study will follow 150 patients with chronic planatar fasciitis operated with PMGR study. The follow up time is 2 years and the study aims at documenting the effect of the surgery with PROMS (patient related outcome measures), MRI (magnetic resonnance imaging) and ankle movement measurements. 26 patient-related baseline factors will also be registered. A regression analysis will be performed to identify factors that may be predictive to the effect of PMGR surgery.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 150
• Est. completion date: March 15, 2026
• Est. primary completion date: March 15, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion criteria:

1. Age 18-75 years.

2. Diagnosis plantar fasciitis verified clinically by orthopaedic surgeon.

3. Diagnosis verified by MRI. MRI criteria: Thickening of the plantar fascia, oedema in the calcaneus, pathological singal changes in the plantar fascia (37)

4. Duration of symptoms must be at least 12 months.

5. An isolated gastrocnemius contracture must be verified with the Silverskiölds test before inclusion.

6. Conventional Physical Therapy must have been tried at least three months without positive effects on symptoms from affected foot.

Exclusion criteria:

1. Previously undergone surgery for plantar fasciitis.

2. Patients with severe talocrural pathology or serious malalignment of foot and ankle

3. Severely reduced peripheral circulation or chronic ulcerations of the foot

4. History of alcoholism, drug abuse, psychological or other emotional problems likely to jeopardize informed consent.

5. Patients with a contraindication/non-compliance for MRI examination.

6. Unable to walk without aid.

7. Not able to read and/or speak a Scandinavian language or English adequately.

Related Conditions & MeSH terms

• Chronic Plantar Fasciitis
• Fasciitis
• Fasciitis, Plantar

Intervention

Procedure:
• Proximal Medial Gastrocnemius Recession
Patients will be operated with PMGR as described by Barouk. No additional procedures will be performed. The surgery will be performed with the patients in a prone position under local anaesthetics. A 3-4 cm transverse skin incision is made in the popliteal fossa, the superficial fascia is opened, and the medial gastrocnemius with its tendon (aponeurosis) is located. The tendon is then cut while lifting it with clamps, and care is taken to cut only the white tendon while sparing the underlying muscle. While performing a dorsiflexion movement of the ankle, careful palpation of the muscle is done to ensure that all tendon strands are cut completely. The incision is closed in layers, and only soft dressings applied. Patients will be instructed to continue the stretching exercises and fully weight-bear from the first postoperative day. If needed, the patients will be allowed to use crutches during the first 2 weeks after surgery. Sutures are removed 2-3 weeks after surgery.

Locations

Country	Name	City	State
Norway	Østfold Hospital Trust	Sarpsborg

Sponsors (1)

Lead Sponsor	Collaborator
Ostfold Hospital Trust

Country where clinical trial is conducted

Norway, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Baseline Patient related factors	The baseline assessment of outcomes and baseline data will be performed no less than two-four weeks before intervention.; Baseline data includes Age, sex, BMI, smoking, medication, diabetes, rheumatologic disease, employment, type of employment, education level, duration of symptoms, previous treatments, activity level, clinical varus/valgus deformity, use of insoles, previous surgeries in affected foot/ankle for other conditions, clinical hallux valgus deformity, symptomatic hallux valgus deformity, taylors bunion, stable/unstable ankle joint, dominant foot, MRI findings (2), X-ray finding (1): Heel spur. Total number of variables: 26 These data will later be used in regression analysis.	Baseline
Primary	Manchester Oxford Foot Questionnaire (MOxFQ)	Patient Related Outcome Measure (PROM) validated for disorders in foot and ankle	Baseline
Primary	Manchester Oxford Foot Questionnaire (MOxFQ)	Patient Related Outcome Measure (PROM) validated for disorders in foot and ankle	6 weeks postoperatively
Primary	Manchester Oxford Foot Questionnaire (MOxFQ)	Patient Related Outcome Measure (PROM) validated for disorders in foot and ankle	12 weeks postoperatively
Primary	Manchester Oxford Foot Questionnaire (MOxFQ)	Patient Related Outcome Measure (PROM) validated for disorders in foot and ankle	1 year postoperatively
Primary	Manchester Oxford Foot Questionnaire (MOxFQ)	Patient Related Outcome Measure (PROM) validated for disorders in foot and ankle	2 years postoperatively
Secondary	VAS (visual analogue scale)	Visual analogue scale for pain during use of affected leg in the last 24 hours. 0 is no pain. 10 is worst pain imaginable.	Baseline, 12 weeks, 1 year, 2 years
Secondary	EQ5D (EuroQol questionnaire )	EQ-5D is a validated generic health-related quality-of-life instrument. It consists of two parts: EQ-5D descriptive part and EQ-5D visual analogue scale. The descriptive part includes five dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression), each with three possible answers ("no problems", "some problems", and "major problems"). EQ5D VAS is a visual analogue scale of self-related overall health, ranging from 0 (worst imaginable health state) to 100 (best imaginable health state	Baseline, 12 weeks, 1 year, 2 years
Secondary	MRI (magnetic resonancd imaging) findings	Thickness of plantar fascia at insertion, pathological signals in the fascia yes/no more, less or same as before, presence of oedema in the calcaneal bone yes/no.	Baseline, 2years
Secondary	Adverse events	infection, nerve injury, thrombosis.	Baseline, 6 weeks, 12 weeks, 1 year, 2 years
Secondary	Ankle movement	Ankle dorsiflexion measured in degrees, through a validated gonimeter	Baseline, 12 weeks, 2 years
Secondary	Gait analysis - Maximal ankle dorsiflexion during stance (degrees)	A sub-group of patients (n= 30) will be offered to be tested in a walking lab, comparing their ankle dorsiflexion during stance pre-and postoperatively. Due to a limited access to this facility, not all patients will be able to perform this test.; - Maximal ankle dorsiflexion during stance (degrees)	Baseline, 3 months
Secondary	Gait analysis (Length of stride. Centimeters)	A sub-group of patients (n= 30) will be offered to be tested in a walking lab, comparing their ankle dorsiflexion during stance pre-and postoperatively. Due to a limited access to this facility, not all patients will be able to perform this test.	Baseline, 3 months
Secondary	Gait analysis Ankle power	A sub-group of patients (n= 30) will be offered to be tested in a walking lab, comparing their ankle dorsiflexion during stance pre-and postoperatively. Due to a limited access to this facility, not all patients will be able to perform this test.	Baseline, 3 months
Secondary	Gait analysis Cadence (steps/minute)	A sub-group of patients (n= 30) will be offered to be tested in a walking lab, comparing their ankle dorsiflexion during stance pre-and postoperatively. Due to a limited access to this facility, not all patients will be able to perform this test.	Baseline, 3 months
Secondary	Gait analysis Maximal external rotation of ankle during stance (degrees)	A sub-group of patients (n= 30) will be offered to be tested in a walking lab, comparing their ankle dorsiflexion during stance pre-and postoperatively. Due to a limited access to this facility, not all patients will be able to perform this test.; Maximal ankle dorsiflexion during stance (degrees); Length of stride. Centimeters; Cadence (steps/minute); Ankle power; Maximal external rotation of ankle during stance (degrees); Knee extension while maximal dorsiflexion of ankle during stance (degrees)	Baseline, 3 months
Secondary	Gait analysis Knee extension while maximal dorsiflexion of ankle during stance (degrees)	A sub-group of patients (n= 30) will be offered to be tested in a walking lab, comparing their ankle dorsiflexion during stance pre-and postoperatively. Due to a limited access to this facility, not all patients will be able to perform this test.	Baseline, 3 months
Secondary	Assessment of treatment success -pain	Likert question: I have pain in the heel pain in the leg that was operated two years ago Answers. 1) Strongly Disagree; (2) Disagree; (3) Neither Agree nor Disagree; (4) Agree; (5) Strongly Agree	at 2 years
Secondary	Assessment of treatment success - physical activity	Likert question:Heel pain prevents me from performing physical acitvity Answers. 1) Strongly Disagree; (2) Disagree; (3) Neither Agree nor Disagree; (4) Agree; (5) Strongly Agree	at 2 years
Secondary	Assessment of treatment success - daily living	Likert question:Heel pain prevents me from performing activities of daily living Answers. 1) Strongly Disagree; (2) Disagree; (3) Neither Agree nor Disagree; (4) Agree; (5) Strongly Agree	at 2 years
Secondary	Assessment of treatment success - other treatments	Likert question:I have pain and/or discomfort in the calf that was operated two years ago Answers. 1) Strongly Disagree; (2) Disagree; (3) Neither Agree nor Disagree; (4) Agree; (5) Strongly Agree	at 2 years
Secondary	Assessment of treatment success - patient acceptable symptom state	I have received other treatments for plantar fasciitis since surgery was performed two years ago YES/NO	at 2 years
Secondary	Assessment of treatment success	If you were to continue having the same level of symptoms in the next few months, would you consider that acceptable.; YES/NO	at 2 years