Kanakadi (utricaria) in children

Clinical Evaluation of Herbal Formulation-Vilva Ilai Kudineer for Kanakadi(utricaria) in Children.

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/06/019570

Enrollment

Registered

2019-06-07

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: L500- Allergic urticaria

Interventions

Intervention1: VILVA ILAI KUDINEER (Internal): Vilva Ilai Kudineer is a single herb formulation in a dosage of 30ml(bd) for 48 days. Control Intervention1: NIL: NIL

Eligibility

Inclusion criteria

Inclusion criteria: Acute and chronic utricaria Wheel formation Itching Erythymatous rashes. Those who are willing to sign in consent form

Exclusion criteria

Exclusion criteria: Fever with rashes Pitriasis rosea Drug eruptions Erythema multiforme other systemic illness Acute bronchospasm

Design outcomes

Primary

Measure	Time frame
Efficacy of the trial drug is measured using utricaria activity scale and improvement in the clinical symptoms is assured.Timepoint: 1-48 days	—

Secondary

Measure	Time frame
Improvement in the reduction of wheel formation,pruritis and prevention of recurrent utricarial rashes.Timepoint: 1-48 days	—

Countries

India

Contacts

Public ContactDr K Vennila

National Institute of Siddha

mmssiddha@gmail.com9444214582

Outcome results

None listed

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