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Instep Plantar Fasciotomy With and Without Gastrocnemius Recession

Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02287714
Enrollment
0
Registered
2014-11-11
Start date
2014-05-31
Completion date
2016-02-29
Last updated
2016-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Equinus Deformity, Plantar Fasciitis

Keywords

Instep plantar fasciotomy

Brief summary

Compare results of Instep Plantar Fascial release with and without gastrocnemius recession

Detailed description

Plantar fasciitis is one of the most common causes of heel pain. Approximately 2 million Americans seek treatment for plantar fasciitis every year, with 10% of the population developing plantar fasciitis over a lifetime. The vast majority of cases respond to conservative care; however, the 5-10% of cases that are recalcitrant to conservative measures may require surgical intervention. Several surgical options do exist and are cited in the literature for treatment of recalcitrant plantar fasciitis. One such approach is the instep plantar fascial release, utilizing an approximately 2-3 cm plantar incision over the prominent fascial band, just distal to the fat pad of the heel. It has been demonstrated that many patients with plantar fasciitis also have an isolated contracture of the gastrocnemius, known as gastrocnemius equinus. Gastrocnemius recession is performed to correct an isolated gastrocnemius contracture and recent studies have demonstrated its successful use in the treatment of recalcitrant foot pain. To date, no prospective studies exist examining the utilization of the gastrocnemius recession in combination with instep plantar fascial release in the treatment of recalcitrant plantar fasciitis. This prospective randomized trial will aim to compare the use of instep plantar fasciotomy both with and without gastrocnemius recession in the treatment of plantar fasciitis.

Interventions

PROCEDUREInstep without gastrocnemius recession

Patient will receive an instep plantar fascial release without gastrocnemius recession.

PROCEDUREInstep with gastrocnemius recession

Patient will receive an instep plantar fascial release as well as gastrocnemius recession.

Sponsors

OhioHealth
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients that have failed conservative treatment for greater than 6 months. * Patients with recalcitrant plantar fasciitis and simultaneous gastrocnemius contracture in the ipsilateral limb. Contracture will be defined as the inability to dorsiflex the ankle past neutral with the knee in extension.

Exclusion criteria

* Adjunctive procedure at the time of surgery. * History of heel spur surgery, plantar fasciotomy or extracorporeal shockwave therapy.

Design outcomes

Primary

MeasureTime frameDescription
Change in American Orthopedic Foot and Ankle Society Scorechange from baseline (within 30 days prior to intervention) AOFAS score at 3 mo, 6 mo, and one yearSubjective and objective measurements which scale a patients' pain and function collected at selected intervals and compared to pre-operatively.

Secondary

MeasureTime frameDescription
Adjunctive treatmentOne yearParticipant chart will be reviewed for any adjunctive treatment required following their surgical intervention
ComplicationsOne yearParticipant chart will be reviewed for any complications that occurred during their one year follow-up, including but not limited to: Recurrence of symptoms, no improvement, infection, tear or rupture of plantar fascia following procedure
Change in Activity levelchange from baseline (within 30 days prior to intervention) activity level at 3 months, 6 months, and one yearA patient submitted survey regarding their activity level and ability to perform those activities pain free.
Change Pain levelchange from baseline (within 30 days prior to intervention) pain level at 3 months, 6 months, and one yearPatients will be asked to submit their pain level utilizing the Visual Analog Scale

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026