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A STUDY ON SIDDHA MEDICINE "KAASAKULANTHAGA MAMATHIRAI(TABLET)" for BRONCHIAL ASTHMA (swasakasam)

A CLINICAL STUDY ON SIDDHA HERBOMINERAL FORMULATION "KAASAKULANTHAGA MAATHIRAI"IN SWAASAKAASAM(BRONCHIAL ASTHMA)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/02/017700
Enrollment
30
Registered
2019-02-18
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: J00-J99- Diseases of the respiratory system

Interventions

Intervention1: Kaasakulanthaga Maathirai (Tablet): Single arm study Control Intervention1: Kaasakulanthaga Maathirai (Tablet).: one Tablet (130 mg),Twice a day,Internal for 5 days.

Sponsors

Ayothidoss Pandithar Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: MODERATE PERSISTANT TYPE OF BRONCHIAL ASTHMA, WEEKLY TWICE OR DAILY SYMPTOMS OF DIFFICULTY IN BREATHING,TIGHTNESS OF CHEST,WHEEZE.EXACERBATION IS TWO OR MORE IN A YEAR,REVERSIBLE BY BRONCHO DILATOR,OBSTRUCTIVE TYPE OF ASTHMA,Asthma sometimes interferes with normal daily activities,Patient who are willing to take radiological investigation and provide blood for lab investigation.Patient who is willing to estimate volume of air forcibly expired after a deep inspiration by using Pulmonary Function Test.

Exclusion criteria

Exclusion criteria: Restrictive lung disease,Tuberculosis,COPD,Lung Carcinoma and other Carcinomas,Status asthmatics,Emphysema,Pleural effusion,Cardiac disease,Hypertension,Renal disease,Diabetic mellitus,Recent abdominal, thoracic, or eye surgery,Symptoms of acute severe illness like Chest pain, nausea, vomiting, high fever, dyspnea,Recent hemoptysis,Pneumothorax,Recent history of abdominal, thoracic, or cerebral aneurysm,Anaemia,Sleep apnoea,Pregnancy,Lactation,Psychological factor.

Design outcomes

Primary

MeasureTime frame
Primary outcome is assessed by comparing the lung volumes and capacities in pre and post treatment pulmonary function test.Timepoint: 5 days

Secondary

MeasureTime frame
Secondary outcome is assessed by comparing the parameters, before and after treatment Relieving of other clinical symptoms.Evaluating clinical lab parameters including Ig E, AEC. Timepoint: 5 days

Countries

India

Contacts

Public ContactDr Hitha Shyam M S

MGR Medical University

drlakshmiramaswamy@gmail.com9444466880

Outcome results

None listed

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