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Application of Plant Protection Products (PPP) in Apple Orchards (aPPPle)

G

German Federal Institute for Risk Assessment

Status

Enrolling

Conditions

Dermal Exposure
Metabolites in Urine
Effekt Biomarker in Blood
Inhalative Exposure

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of the aPPPle pilot study is to test feasibility and generate first results in preparation for a main study. The aPPPle study will investigate the exposure of operators, workers and residents to plant protection products (PPP) and potential physiological effects on blood biomarkers. The target plants are apple crops, as application occurs at higher altitudes and therefore higher drift/exposure is expected compared to ground-level application. The substances to be investigated are acetamiprid (an insecticide) and dithianon and dodine (two fungicides).

Enrollment

16 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • belonging to one of the defined study groups
  • over 18 years of age at the time of recruitment
  • person can understand the language and content of the study requirements
  • person is capable of consenting to participate in the study and has given written consent to participate in the aPPPle study
  • person has health insurance

Exclusion Criteria for residents and control:

person has direct professional contact with the tested substances acetamiprid, dithianon or dodine

Trial design

16 participants in 4 patient groups

Operators
Description:
People who apply plant protection products to apple crops.
Workers
Description:
People who do manual work in apple cultivation, like pruning or harvesting.
Residents
Description:
People whose place of residence is adjacent to the orchard under investigation.
Control
Description:
People whose place of residence is at least 10 km away from agricultural apple orchards and a maximum of 150 km away from the apple orchard under investigation.

Trial contacts and locations

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Central trial contact

Dr. Anna Lechner; Prof. Dr. Cornelia Weikert

Data sourced from clinicaltrials.gov

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