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Digitalisation of personalised medication in primary care

Digitalisation of personalised medication in primary care - DIPP – Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036092
Enrollment
250
Registered
2025-02-25
Start date
2025-10-20
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Polypharmacy

Interventions

Group 1: Test group: digitally supported pharmacotherapy decisions considering the pharmacogenetic profiles of patients. The treating physicians are provided with the PGXperts PGx profile. The physici

Sponsors

PGXperts GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients from general practices who take more than four medications. 2. Willingness to provide a blood sample for molecular genetic laboratory testing. 3. Patients with possible medication-related issues, such as adverse drug reactions, side effects, lack of efficacy, or non-specific symptoms, in whom the treating physician considers a review of the overall medication to be necessary.

Exclusion criteria

Exclusion criteria: 1. Bone marrow, liver or kidney transplant. 2. Blood transfusion in the last four weeks. 3. Cognitive impairment that causes the investigator to consider the patient unsuitable for inclusion in the study. 4. Cancer treated with chemotherapy within the last five years. 5. Insufficient knowledge of German, such that the patient cannot, in the opinion of the investigator, communicate sufficiently. 6. Acute onset of symptoms without any recognisable connection to the medication. 7. Acute or subacute symptoms requiring immediate adjustment of medication.

Design outcomes

Primary

MeasureTime frame
Difference in EQ-5D-VAS score at week 4 compared to baseline

Secondary

MeasureTime frame
- Difference from baseline in the EQ-5D-5L index after week 4 - Difference from baseline in the symptom total score (SSS) after four weeks.

Countries

Germany

Contacts

Public ContactPaola Zambrano

PGXperts GmbH

dipp.studie@pgxperts.com+49 (0) 911 979 10 850

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 29, 2026