Randomised Controlled Clinical Trials of the Effect of Therapeutic Hookworm Infection in Allergic Rhinoconjunctivitis
Primary Purpose
Rhinitis, Allergic, Perennial, Hayfever, Allergy
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Infection with hookworm larvae
Sponsored by
About this trial
This is an interventional treatment trial for Rhinitis, Allergic, Perennial focused on measuring immune system, infection, allergic rhinitis
Eligibility Criteria
Inclusion Criteria: Symptoms of allergic rhinitis Measurable airway responsiveness to AMP Negative hookworm serology Positive skin prick tests to D.pteronyssinum, cat fur or grass pollen Exclusion Criteria: History of asthma History of anaemia History of severe allergic reaction or anaphylaxis Possible or planned pregnancy
Sites / Locations
- University of Nottingham
Outcomes
Primary Outcome Measures
Maximum change from baseline in airway responsiveness to adenosine 5'-monophosphate (AMP) during the lung migration phase of hookworm infection.
Secondary Outcome Measures
Change from baseline in rhinoconjunctivitis quality of life questionnaire score
allergen skin wheal response
mean daily peak flow
total- and specific serum IgE titres
acidic mammalian chitinase, cytokine profiles, other inflammatory markers
occurrence of adverse effects
Full Information
NCT ID
NCT00232518
First Posted
September 30, 2005
Last Updated
May 4, 2007
Sponsor
University of Nottingham
1. Study Identification
Unique Protocol Identification Number
NCT00232518
Brief Title
Randomised Controlled Clinical Trials of the Effect of Therapeutic Hookworm Infection in Allergic Rhinoconjunctivitis
Official Title
Randomised Controlled Clinical Trial of the Effect of Therapeutic Hookworm Infection in Allergic Rhinoconjunctivitis
Study Type
Interventional
2. Study Status
Record Verification Date
April 2005
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University of Nottingham
4. Oversight
5. Study Description
Brief Summary
There has been considerable debate over the last 30 years about the interaction between asthma and parasitic infection. It has been suggested that at least part of the reason for the increasing prevalence of asthma in the developed world is a decrease in parasite infections resulting from improved living conditions with economic development. Our previous studies in Ethiopia suggest that hookworm infection may be particularly important in this process.
To establish definitively whether parasites can protect against allergic disease, and specifically asthma, ultimately requires a randomised clinical trial of parasite infection in patients with asthma. We, the researchers at the University of Nottingham, have completed a study in normal volunteers to establish the dose of hookworms necessary to generate infection at the level shown to be protective in population surveys, and shown that infection is well tolerated. We now propose two randomised placebo-controlled double blind clinical trials. The first will test the effectiveness of hookworm infection in reducing symptoms in allergic patients with rhinitis, and will also serve to allow us to check the likely safety of hookworm infection in asthma. Assuming that the results of this study are favourable, we will then carry out a trial of hookworm infection in asthma. We will also take the opportunity during both of these studies to investigate the cellular mechanisms of the effect of hookworm infection on the immune system.
Detailed Description
Epidemiological evidence suggests that human hookworm infection is associated with a reduced risk of asthma and allergic disease. This association is potentially important not only to understanding the aetiology of asthma and allergic disease, but also because it suggests that hookworms or their products might be therapeutically effective in these conditions. To test the hypothesis that hookworms protect against asthma ultimately requires a clinical trial.
We have carried out a dose-ranging study to establish the dose of hookworm larvae necessary to generate infection at the intensity shown to be protective in epidemiological studies, with acceptable side effects, and now propose to test the effect of 12 weeks of hookworm infection at this level of intensity in two randomised placebo controlled clinical trials. The first will be in patients with allergic rhinoconjunctivitis, to determine whether hookworm infection improves rhinitis symptoms and also, because these patients will have measurable airway responsiveness, to determine whether airway responsiveness changes during the lung migration phase of the hookworm life cycle. If this study confirms that hookworm infection does not increase airway responsiveness, we will proceed to a similar trial in patients with asthma.
In both studies we will also measure a range of relevant immunological parameters to explore the relation between these parameters and expression of the allergic and asthmatic phenotypes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rhinitis, Allergic, Perennial, Hayfever, Allergy
Keywords
immune system, infection, allergic rhinitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
30 (false)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
Infection with hookworm larvae
Primary Outcome Measure Information:
Title
Maximum change from baseline in airway responsiveness to adenosine 5'-monophosphate (AMP) during the lung migration phase of hookworm infection.
Secondary Outcome Measure Information:
Title
Change from baseline in rhinoconjunctivitis quality of life questionnaire score
Title
allergen skin wheal response
Title
mean daily peak flow
Title
total- and specific serum IgE titres
Title
acidic mammalian chitinase, cytokine profiles, other inflammatory markers
Title
occurrence of adverse effects
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Symptoms of allergic rhinitis
Measurable airway responsiveness to AMP
Negative hookworm serology
Positive skin prick tests to D.pteronyssinum, cat fur or grass pollen
Exclusion Criteria:
History of asthma
History of anaemia
History of severe allergic reaction or anaphylaxis
Possible or planned pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Britton
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David Prichard
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Nottingham
City
Nottingham
ZIP/Postal Code
NG5 1PB
Country
United Kingdom
12. IPD Sharing Statement
Learn more about this trial
Randomised Controlled Clinical Trials of the Effect of Therapeutic Hookworm Infection in Allergic Rhinoconjunctivitis
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