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A clinical study on kuthikaal vatha kudineer and Nochi ilai kattu for kuthikaal vatham(Calcaneal spur)

An open labelled double arm non randomised phase II clinical trial to compare the efficacy of VARMA MANIPULATION with KUTHIKAAL VATHA KUDINEER (internal)and NOCHI ILAI KATTU(external)in the treatment of KUTHIKAAL VATHAM

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026778
Enrollment
40
Registered
2020-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M216- Other acquired deformities of foot

Interventions

Intervention1: Varma manipulation: varma manipulation for 48 days Intervention2: Varma manipulation: Varma manipulation for 48 days Intervention3: Varma Manipulation: Varma manipulation for 48 days In

Sponsors

Government siddha medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patient having symptoms of sharp pain like knife in the heel when standing up in the morning ,a dull ache in the heel throughout the rest of the day patient who are willing to give radiological investigation and provide blood for lap invetigation patient willing to sign the informed consent stating that he/she will conscientiously sick to the treatment during 48 days but can option out of the trial of his/her own conscious giscretion

Exclusion criteria

Exclusion criteria: fracture of the foot ,pagets disease affecting the calcanium,rupture of Achilles tendon,systemic disorder like TB,DM,HIV,Leukaemia

Design outcomes

Primary

MeasureTime frame
Assessment of change from baseline in Universal Pain Assessment scale at day 48 between GroupI(Varma therapy)and GropII(Medicine and Varma therapy) comparison of efficacy in patient GroupI and GroupIITimepoint: 48 days

Secondary

MeasureTime frame
Assessment of quality of life by Universal Pain score scale.Assessment of safety parametersTimepoint: 48 days

Countries

India

Contacts

Public ContactDr S SUJATHA

GOVT SIDDHA MEDICAL COLLEGE

sujatharajasekar66@gmail.com9445816706

Outcome results

None listed

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