Skip to content

A comparative efficacy evaluation of ultrasound-guided pulsed radiofrequency treatment in the gastrocnemius in managing plantar heel pain: A randomized and controlled trial

A comparative efficacy evaluation of ultrasound-guided pulsed radiofrequency treatment in the gastrocnemius in managing plantar heel pain: A randomized and controlled trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003410
Enrollment
Unknown
Registered
2013-07-11
Start date
2013-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

plantar heel pain

Interventions

miniscaple needle:miniscaple needle
radiofrequency:radiofrequency
sham miniscaple needle:sham miniscaple needle
sham radiofrequency:sham radiofrequency
Gastrocnemius tension:Gastrocnemius tension

Sponsors

Department of pain management, Renji Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged >=18 years; history of plantar heel pain for more than one months; first step pain during the previous week rated at least 2 cm on a 10 cm visual analogue scale (VAS); clinical diagnosis of plantar heel pain in accordance with the Clinical Guidelines linked to the International Classification of Function, Disability, and Health from the Orthopaedic Section of the American Physical Therapy Association; With palpable trigger points in the gastrocnemiusInformed consent was obtained from all participantsdid not accept other physical or chemical treatments.

Exclusion criteria

Exclusion criteria: pregnancy; the presence of coagulopathy or the use of anticoagulants (except for acetylsalicylic acid at dosages up to 325 mg/day); an inability to understand instructions or complete a questionnaire; plantar heel pain caused by in?ammatory, malignant, or autoimmune disease; the presence of a chronic medical condition that might preclude participation in the study such as: malignancy, systemic inflammatory disorders, neurological abnormalities, sciatica, and/or chronic pain; a history of surgery to the plantar fascia in the past four weeks; a known hypersensitivity to metals?

Design outcomes

Primary

MeasureTime frame
Visual analogue scale (VAS) - 'First-step’ pain;Foot Health Status Questionnaire (FHSQ) - pain;

Secondary

MeasureTime frame
Foot Health Status Questionnaire (FHSQ)– foot function;

Countries

China

Contacts

Public ContactYongjun Zheng
zhengyongjun1971@126.com+86 13918753886

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026