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Biodosimetry compared to physical dosimetry in nuclear medicine imaging and radionuclide therapies

Biodosimetry compared to physical dosimetry in nuclear medicine imaging and radionuclide therapies

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00038771
Enrollment
43
Registered
2026-02-24
Start date
2024-07-23
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

C61 E00-E07

Interventions

Group 1: Molecular biological analysis of the blood samples obtained. Changes in gene expression, the epigenome, and chromatin structure, DNA damage response, and blood count are examined. Saliva samp

Sponsors

Universitätsklinikum Augsburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Written consent to participate in the study • Age > 18 years • Capacity to consent • Medically justified indication for the use of open radioactive substances by the attending physician

Exclusion criteria

Exclusion criteria: - Pregnant or breastfeeding women - Minors (< 18 years of age) and patients with mental illnesses - Patients who are unable to provide written consent to participate in the study. - Age < 18 years - Pregnancy - Lack of written consent from the patient

Design outcomes

Primary

MeasureTime frame
The primary objective of this in vivo project is to investigate whether various biological changes can also be detected in the context of radiation exposure during the use of open radioactive substances. This is done by taking saliva and blood samples.

Countries

Germany

Contacts

Public ContactChristian Pfob

Universitätsklinikum Augsburg

Studien.Nuk@uk-augsburg.de+498214002067

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026