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临床试验/ISRCTN98064931
ISRCTN98064931已完成Unknown

In patients with chronic plantar fasciitis, does post-injection load restriction compared to no load restriction improve recovery time and pain reduction following autologous whole-blood injection?

sak University0 个研究点目标入组 152 人开始时间: 2024年8月9日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
152

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Age Range: 20 to 65 years old
  • 2. Diagnosis: Diagnosed with plantar fasciitis that has not responded to at least two months of conservative treatment
  • 3. Treatment History: No prior history of autologous whole-blood injections for plantar fasciitis
  • 4. Consent: Willingness to provide informed consent for participation in the study
  • 5. Mobility: Capable of using Canadian crutches if assigned to the load restriction group
  • 6. Health Status: No significant systemic diseases or conditions affecting the foot or plantar fascia

排除标准

  • 1. Heavy Labor Employment: Participants who are employed in jobs involving heavy physical labor
  • 2. Use of Immunomodulatory Drugs: Individuals who are currently using immunomodulatory medications
  • 3. Previous Injection History: Patients with a history of previous injections for plantar fasciitis
  • 4. Bilateral Plantar Fasciitis: Individuals diagnosed with plantar fasciitis in both feet
  • 5. Previous Foot Surgery: Patients who have undergone foot surgery in the past
  • 6. Local Anesthetic Sensitivity: Individuals with known sensitivity or adverse reactions to local anesthetics
  • 7. Rheumatological Diseases: Participants with diagnosed rheumatological conditions
  • 8. Autoimmune/Neuropathic Diseases: Individuals with autoimmune or neuropathic disorders

研究者

发起方
sak University

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