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A clinical study on Kanduparangi Chooranam in the management of Iya Iraippu Noi (Bronchial Asthma)

A Prospective Open-labelled, Non-Randomized, Phase -II Clinical trial of Kanduparangi Chooranam in the management of Iya Iraippu Noi (Bronchial Asthma)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019120
Enrollment
60
Registered
2019-05-14
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: J459- Other and unspecified asthma

Interventions

Intervention1: Kanduparangi Chooranam: 60 mg/Kg/BW/twice a day A/F 30 days Control Intervention1: NIL: NIL

Sponsors

Government Siddha Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient with the symptoms of dry cough, recurrent attacks of dyspnoea,hoarseness of voice,frequent hemming,tightness of chest, profuse sweating & wheezing 2)H/o allergens, sneezing. 3)Patients who are willing to take radiological investigation and provide blood for lab investigation. 4)Patients who are willing to estimate volume of air forcibly expired after a deep inspiration by using Mini-Peak flow meter and PEFR below normal range from 250L/min to 150 l/min for men, from 200L/min to 100 L/min for women, for those patients are included. 7)Patients who are willing to do Spirometer study - To estimate Pulmonary Function Test (PFT)

Exclusion criteria

Exclusion criteria: 1)Pregancy 2)Lactating mother 3)Cardiac disease 4)Renal disease 5)Tuberculosis 6)Chronic bronchitis 7)Status asthmaticus 8)Diabetes mellitus 9)Auto immune disease.

Design outcomes

Primary

MeasureTime frame
If during treatment or after treatment reduction of the following symptoms 1.Dry cough 2.Recurrent attacks of dyspnoea 3.Hoarseness of voice 4.Frequent hemming 5.Tightness of chest 6.Profuse sweating 7.Wheezing. Timepoint: 30 days

Secondary

MeasureTime frame
1.Evaluation of physicochemical, phyto chemical, bio chemical, pharmacological activities of â??Kanduparangi Chooranamâ??. 2.Evaluation of siddha parameters (including Envagai thervu)changes in â??IYA IRAIPPU NOI â?? during trial period. 3.Evaluation of modern parametric changes in â??IYA IRAIPPU NOIâ??. 4.Evaluation of safety profile for acute and sub-acute toxicity of trial drug. Timepoint: 30 days

Countries

India

Contacts

Public ContactDr SJustus Antony MD PhD

Government Siddha Medical College and Hospital

drmanoharan25@gmail.com9443886700

Outcome results

None listed

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