Clinical trial to evaluate the efficacy of kana kudineer in children for Vali Kanam(Acute pharyngitis)

Phase II an open single group non randomized study on valikanam (Acute pharyngitis) to evaluate the official Siddha formulation kana kudineer-In children of both sex aging between 3-12 years attending opd at Anna hospital

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/11/022196

Enrollment

Registered

2019-11-27

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: J02- Acute pharyngitis

Interventions

Intervention1: Kana kudineer: 15-30 ml Twice a day 14 days Control Intervention1: Nil: Nil

Eligibility

Inclusion criteria

Inclusion criteria: 3-12 years Fever Sore throat / throat pain Hoarseness of voice Cough Pharyngeal Tendulkar erythema Cervical adenopathy Rhinitis

Exclusion criteria

Exclusion criteria: Peritonsillar abscess H/O Rheumatic fever Diptheria Inductive mononucleosis

Design outcomes

Primary

Measure	Time frame
Reduction in center score Reduction in clinical symptoms like fever, throat pain, sore throat and coughTimepoint: 14 days	—

Secondary

Measure	Time frame
It is assessed by comparing the safety parameters before and after treatmentTimepoint: 14 days	—

Countries

India

Contacts

Public ContactDr Kalishwari B

Government Siddha Medical College

ranimoorthybsms19@gmail.com9442286863

Outcome results

None listed

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