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Gastrocnemius Recession vs. Conservative Treatment for Chronic Plantar Fasciitis

Gastrocnemius Recession vs. Conservative Treatment for Chronic Plantar Fasciitis. A Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02116478
Enrollment
40
Registered
2014-04-17
Start date
2014-08-31
Completion date
2022-06-30
Last updated
2021-03-15

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

Conditions

Plantar Fasciitis

Keywords

plantar fasciitis, gastrocnemius recession

Brief summary

The purpose of the study is to compare the clinical results for patients suffering from plantar fasciitis treated with gastrocnemius recession vs. conservative treatment.

Detailed description

All patients will be instructed in stretching exercises. Half of the patients will be randomized to proximal medial gastrocnemius recession. All patients will be followed for 1 year. Additional long term follow-up will be 6 years after inclusion

Interventions

PROCEDUREsurgical proximal medial gastrocnemius recession

proximal medial gastrocnemius recession

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Symptoms of plantar fasciitis lasting more than 12 months. * Isolated gastrocnemius contracture

Exclusion criteria

* No previous surgery to foot or ankle * No active arthritis

Design outcomes

Primary

MeasureTime frameDescription
Change in American Orthopaedic foot and ankle society (AOFAS) ankle-hindfoot score1 year and 6 years postoperativeThe change in AOFAS from baseline to follow-up, as well as the difference between the groups treated non-operatively and operatively will be reported on a 0-100 scale.

Secondary

MeasureTime frameDescription
0-10 points Visual analog pain score1 year and 6 years postoperativeDifference in pain between groups will be reported on 0-10 points visual analog scale

Other

MeasureTime frameDescription
Short form-36 (SF-36)1 year and 6 years postoperativeDifference in subgroup parameters between baseline and follow-up as well as between group differences will be reported

Countries

Norway

Outcome results

None listed

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