Bronchial asthma.
Conditions
Interventions
(Active) study group: Subcutaneous injections were given in deltoid region, and increasing volumes of the researched vaccine at different doses (20, 200, 2,000 and 20,000 UB/ml) for 13 weeks during th
Injections, Subcutaneous
Placebos
Sponsors
National Biopreparations Center (BIOCEN)
Eligibility
Sex/Gender
All
Age
16 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Asthmatic allergic patients with positive responses during the preliminary survey in the following aspects: family and personal history of atopy, clinical symptoms only triggered when exposed to dust at home, mainly indoors, when getting up in the morning or going to bed at night. 2. Skin test positive to B. tropicalis allergenic extract, 20,000 BU/ml VALERGEN-BT. The response to the allergen under study is predominant when compared to that obtained with other mites. 3. Patients included in the study will be patients clinically diagnosed as extrinsic asthmatics who, according to the clinical-therapeutic identification booklet, are classified as mild or moderate persistent patients in keeping with the International Agreement on Asthma Diagnosis and Treatment. 4. Age between 16 and 45 years. 5. Any sex and race. 6. Patients expressing their consent in writing to participate in our trial.
Exclusion criteria
Exclusion criteria: 1. Patients not giving their consent in writing to participate in our trial. 2. Patients on allergenic extract immunotherapy during the two preceding years. 3. Patients classified as intermittent or severe persistent asthmatics after being interviewed. 4. Patients with a diagnosed autoimmune disease of any kind. 5. Generalized severe eczema. 6. Patients with diagnosed tumoral disease. 7. Patients on betablocker treatment. 8. Patients with psychiatric disorders. 9. Patients not cooperating with treatment. 10. Patients who, at least one year before the study, needed immunostimulant or immunosuppressor treatment (no corticosteroids), including interferon and cyclosporine A. 11. Pregnancy and breastfeeding. 12. Adrenalin-contraindicated patients (high blood pressure). 13. Patients who, at least one year before the study, were under non-conventional treatments such as: Vimang, Aloe, ozone, banana capsules.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Score by symptoms, score by drug consumption, cutaneous reactivity (Ch10 value: relative allergen concentration causing in the patient a bump similar to the one caused by a 10 mg/ml HCL histamine solution (54.3 mmol/l base histamine). Measuring time: 6 months and 1 year. | — |
Secondary
| Measure | Time frame |
|---|---|
| General evaluation (depends on symptoms, medication, respiratory function, Ch10). Measuring time: 6 months and 1 year. | — |
Countries
Cuba
Contacts
Public ContactRaul Castro Almarales
National Biopreparations Center (BIOCEN)
Outcome results
None listed