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Use of BTPB repertory in managing bronchial asthma cases

Clinical utility of BTPB in management of bronchial asthma a prospective single arm study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105559
Enrollment
30
Registered
2026-03-06
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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: Individualized homoeopathic medicine based on BTPB: Patients fulfilling the inclusion and exclusion criteria will be enrolled in the study after obtaining written informed consent. Deta

Sponsors

Dr Shailender Singh Rawat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients presenting with clinical signs and symptoms consistent with bronchial asthma 2 Patients with a confirmed diagnosis of bronchial asthma based on clinical history and or diagnostic tests 3 Patients on conventional treatment for bronchial asthma 4 Patients who are willing to participate and provide written informed consent

Exclusion criteria

Exclusion criteria: 1 Patients diagnosed with severe persistent asthma with significant restriction of daily activities 2 Patients experiencing status asthmaticus 3 Patients with serious complications or uncontrolled or life threatening systemic illnesses like cardiac failure or uncontrolled diabetes or renal or hepatic failure 4 Pregnant women and lactating mothers 5 Individuals with a history of substance abuse or dependence 6 Patients unwilling or unable to provide informed consent or participate in the study procedures 7 Individuals with a self reported immune compromised state like HIV or ongoing immunosuppressive therapy

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study will be the change in the Asthma Control Test ACT score from baseline to the end of the study periodTimepoint: 4 weeks

Secondary

MeasureTime frame
The secondary outcome of the study will be assessed using the Asthma Quality of Life Questionnaire AQLQ S developed by Elizabeth JuniperTimepoint: Baseline to 6 months

Countries

India

Contacts

Public ContactDr Shailender Singh Rawat

State National Homoeopathic Medical College And Hospital

dr.neelam1968@rediffmail.com7317066643

Outcome results

None listed

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