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Hymenoptera Sting AllergyZU-HVA-001NCT00742794

Frequency of Hymenoptera-stings in Patients Under Allergen-Specific Immunotherapy (SIT)

An observational study of Hymenoptera Sting Allergy, run by University of Zurich at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In Switzerland, 3.5% of the population are suffering from hymenoptera venom allergy. The only causal treatment of hymenoptera alelrty is venom specific immunotherapy. There are however several reasons, which question the relatively broad application of this expensive treatment. Read more about this study

Who is it for?
Ages 5 to 90 years
Conditions the study is for
Hymenoptera Sting Allergy
What is being tested?
Observation
How many people
200 participants
Where
1 siteSwitzerland
Study dates
Aug 2008to Aug 2010
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 5 to 90 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Hymenoptera sting allergic patients under allergen specific immunotherapy

Who may be able to join

  • Bee and/or Wasp allergic patients treated by SIT

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • Study site

    Zurich

Other trials in Switzerland

About this study

Official title: Frequency of Hymenoptera-stings in Patients Under and After Allergen-specific Immunotherapy: a Retrospective Data-analysis Considering Socio-economic Aspects

In Switzerland, 3.5% of the population are suffering from hymenoptera venom allergy. The only causal treatment of hymenoptera alelrty is venom specific immunotherapy. There are however several reasons, which question the relatively broad application of this expensive treatment. That's why we aim at investigating the actual risk for hymenoptera stings in patients undergoing allergen specific immunotherapy against hymenoptera sting allergy

Being tested
Observation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ObservationOther

    Observation of sting frequency

Study groups in NCT00742794
Study groupRoleWhat they receive
1Hymenoptera sting allergic patients under immunotherapy
Receives: Other: Observation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Aug 2008 (estimated)
  2. Study startAug 2008
  3. Study completionAug 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00742794
Sponsor's protocol ID
ZU-HVA-001
Acronym
ZU-HVA-001
Status last verified
Sep 2008
First submitted
27 Aug 2008
Last updated
19 Aug 2010
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Hymenoptera Sting Allergy, run by University of Zurich at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Aug 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Aug 2010; AzTrials last refreshed its copy on 8 Nov 2026.

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