Skip to main content
Clinical Trials/CTRI/2021/05/033429
CTRI/2021/05/033429
Completed
Phase 2

A controlled clinical study to evaluate the efficacy of murivenna kwath iontophoresis, normal saline iontophoresis, murivenna kwath parishek and the allopathic treatment in the management of vata kantaka w.s.r plantar fasciitis

All India Institute of Ayurveda0 sites25 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: M709- Unspecified soft tissue disorder related to use, overuse and pressure
Sponsor
All India Institute of Ayurveda
Enrollment
25
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
April 14, 2022
Last Updated
3 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Pain in the heel and foot.
  • ï?· Difficulty in walking.
  • 1\. Patients between the age group of 20\-65 years.
  • 2\. Patients of both genders.
  • 3\. Patients suffering from chronic plantar fasciitis.
  • 4\.Chronicity of 6 weeks to 5 years will be included

Exclusion Criteria

  • 1\. Local infection and osteoporotic bony pain.
  • 2\. Sarcoma and any other type of tumour pressing on tendon.
  • 3\. Fracture of calcaneus and Ankle joint bone.
  • 4\. Patients suffering from Rheumatoid Arthritis \& Gout.
  • 5\. Retrocalcaneal pain
  • 6\. Insensate foot
  • 7\. Pes planus
  • 8\. Pes cavus
  • 9\. Tarsal tunnel syndrome
  • 10\. H/O injury to heel

Outcomes

Primary Outcomes

Not specified

Similar Trials