A clinical trail to study the effects of karappan kudineer chooranam (internal) and karappan ennai (external ) in patients with sattai karappan

An open clinical study to evaluate the clinical efficacy of siddha sasthric formulation karappan kudineer chooranam (internal ) and karappan ennai (external )for the treatment of sattai karappan

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/07/014869

Enrollment

Registered

2018-07-13

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: null- sattai karappan

Interventions

Intervention1: Karappan kudineer chooranam(internal)karappan ennai(external): 3-7 years 30ml,7-12 years 60ml,twice a day (morning and evening)internally and Oil-externally. Control Intervention1: not

Eligibility

Inclusion criteria

Inclusion criteria: Patient with appropriate symptoms of intense itching erythema papules papulovesicles crusted lesion all over the body ulceration exudation constipation

Exclusion criteria

Exclusion criteria: children above 12 years scabies psoriasis secondary bacterial infection nummular dermatitis contact dermatitis seborric dermatitis furunculosis photo dermatitis neuro dermatitis

Design outcomes

Primary

Measure	Time frame
the therapeutic efficacy of trial drug Karappan kudineer chooranam(internal)karappan ennai (external)on Sattai karappanTimepoint: 21 days	—

Secondary

Measure	Time frame
Evaluation of siddha diagnostic parametersTimepoint: 21 days	—

Countries

India

Contacts

Public ContactA AMMU

goverment siddha medical college and hospital palayamkottai

dr.dks2012@gmail.com9442048801

Outcome results

None listed

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