| Registry | NCT00917488 |
|---|---|
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional; non randomized, single group, masking: none, diagnostic |
| Enrollment | 27 (Actual) |
| Sponsor | Laboratorios Leti, S.L. (Industry) |
| Conditions | Rhinitis, Allergic, Seasonal, Conjunctivitis, Allergic |
| Interventions | Standardization of allergenic extract (Gly. domesticus) (Other) |
| Dates | start 2009-05-01, primary completion 2010-05-01, completion 2010-07-01, first posted 2009-06-10, last updated 2011-06-20 |
| Locations | 1 site in Spain |
Related Papers Related Patents Related Grants Related Experts
All trials for Rhinitis, Allergic, Seasonal All trials for Conjunctivitis, Allergic All trials of Standardization of allergenic extract (Gly. domesticus)
The main purpose of the trial is to prove the therapeutic value of the product and enable an effective and safe dosage schedule to be recommended
The objective of this study is to determine the biologic activity of a Glycyphagus domesticus allergen extract in histamine equivalent prick (HEP) units, in order to be used as in-house reference preparation (IHRP).
The skin testing procedure, based on the Nordic Guidelines is the reference method for the biological calibration of in-House Reference Preparations (IHRP). The method is not intended for routine testing of allergen extracts. The use of this procedure is the basis for the definition of biological activity units: "the activity of an allergen extract is 10,000 Biological Units (BU) per ml (10 HEP per ml), when the extract provokes an specific skin reaction in the median sensitive patient with a wheal of the same size as a wheal provoked by a positive reference solution consisting of histamine 54.3 mmol/l (for example histamine dihydrochloride 10 mg/ml), when both solutions are administrated using the same technique (prick testing) on at least 20 individuals who are clinically allergic and cutaneously reactive to the allergen concerned".
| Arm | Type | Interventions | Description |
|---|---|---|---|
| A | Experimental | Other: Standardization of allergenic extract (Gly. domesticus) | Four concentrations of Glycyphagus domesticus allergen extract, together with a positive and negative control, using 10 mg/ml histamine dihydrochloride solution and a glycerinated phenol saline solution, respectively, was tested in every patient in duplicate on the volar surface of the forearm. |
Sex: All, ages: 18 Years to 50 Years
Subject inclusion criteria: 1. A documented positive case history with inhalation allergy (rhinitis and/or rhinoconjunctivitis and/or asthma) related to Glycyphagus domesticus. 2. Positive skin prick test with an available preparation of the same allergen extract (a wheal major diameter of at least 3 mm) and/or a positive test for specific IgE. 3. Mean of the areas of the wheals provoked by histamine dihydrochloride (10 mg/ml) ≥ 7 mm2. 4. Age ≥ 18 years and ≤ 50 years 5. Subject can be male or female 6. Subject must be capable of providing written informed consent Subject exclusion criteria: 1. Subjects should not be excluded due to low or high sensitivity to Glycyphagus domesticus. 2. Immunotherapy in the past 2 years with an allergen preparation known to interfere with the allergens to be tested. 3. Use of drugs that may interfere with the skin reactions. 4. Pregnancy, dermographism, atopic dermatitis (locally at the test site), urticaria. 5. Any disease which prohibits the use of adrenaline (hyperthyroidism, arterial hypertension, cardiopathy, etc.) 6. Lack of cooperation which may interfere with the study, or subjects with severe psychiatric, psychological or neurological disorders.
| Facility | City | Country | Status |
|---|---|---|---|
| Clinica Dr. Lobatón | Cadiz, Cadiz | Spain |