management of plantar fasciitis by ayurvedic kwath iontophoresis

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

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/05/033429

Enrollment

Registered

2021-05-06

Start date

Unknown

Completion date

Unknown

Last updated

2022-11-21

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

Conditions

Health Condition 1: M709- Unspecified soft tissue disorder related to use, overuse and pressure

Interventions

Intervention1: murivenna kwath: Murivenna kwath IONTOPHORESIS will be given for 20 mins for 7 days Normal saline IONTOPHORESIS will be goven for 20 mins for 7 days Murivenna kwath parishek will be giv

Eligibility

Inclusion 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

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 11. Acute plantar fasciitis.

Design outcomes

Secondary

Measure	Time frame
to record any complications if found during procedure to asses quality of lifeTimepoint: 60 days	—

Primary

Measure	Time frame
Relief in Heel pain in Vata Kantaka (Plantar Fasciitis). Timepoint: 60 days	—

Countries

India

Contacts

Public ContactPreeti Singh

All India Institute of Ayurveda

drvyasayu@gmail.com8368104072

Outcome results

None listed

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