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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02255136 |
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Date of registration:
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15/02/2012 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Efficacy Study of Homeopathic Medicines in Treatment of Allergic Rhinitis and/or Induced Bronchial Asthma
SBRCTHILARBA |
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Scientific title:
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An Evidence-based Single-blind Randomized Controlled Trial Searching for the Efficacy of Homoeopathic Medicines in Reducing Serum Levels of Cytokines (IL - 10, 13) and Immunoglobulin E in Allergic Rhinitis and/or Induced Bronchial Asthma |
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Date of first enrolment:
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March 2012 |
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Target sample size:
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100 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02255136 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Participant).
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Phase:
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N/A
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Countries of recruitment
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India
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Contacts
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Name:
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Shubhamoy Ghosh, MD(Hom) |
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Address:
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Telephone:
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Email:
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Affiliation:
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Lecturer of the Department of Pathology & Microbiology |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Age between 5 and 65 years
- Both sexes
- Atopic: reactive to allergens with positive skin prick test (SPT) results and/or
eosinophilia
- More than 1 year history of allergic rhinitis and/or induced bronchial asthma
Exclusion Criteria:
- Nasal abnormalities causing obstruction, e.g. nasal polyp(s), deviated septum etc.
- Previous homoeopathic immunotherapy for allergic rhinitis
- Allergen avoidance in past 6 weeks
- Away from usual environment for more than 1 week during trial
- Severe asthma cases as detected clinically
- Respiratory infection
- Severe concomitant disease
- Pregnancy, breast feeding, or likelihood of pregnancy
- Oral or parenteral steroids and/or decongestant in past 6 months
- Conventional desensitization in past 3 months
Age minimum:
5 Years
Age maximum:
65 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Rhinitis; Allergic, With Asthma
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Intervention(s)
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Other: Placebo
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Other: Individualized homeopathic medicines
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Primary Outcome(s)
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Serum Interleukin 10 and 13 level
[Time Frame: 1 year]
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Secondary Outcome(s)
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Incidence of adverse events if any
[Time Frame: 1 year]
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Secondary ID(s)
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793/MBHMCH/CH/Adm/01/2011
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CTRI/2012/02/002419
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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