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The DIPAK Observational Cohort Study: a multi-center, longitudinal, observational study to investigate renal disease progression and association of disease biomarkers with renal disease progression and ADPKD-related outcomes.

The DIPAK Observational Cohort Study: a multi-center, longitudinal, observational study to investigate renal disease progression and association of disease biomarkers with renal disease progression and ADPKD-related outcomes. - The DIPAK Observational Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47875
Enrollment
1000
Registered
2013-02-04
Start date
2013-06-04
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Autosomal Dominant Polycystic Kidney Disease or polycystic kidney disease polycystic kidney disease

Interventions

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis of ADPKD, based upon the modified Ravine criteria or documented by treating nephrologist or internist. 2. Age 18 years and older. 3. Providing informed consent.

Exclusion criteria

Exclusion criteria: • Patients, who are unlikely to adequately comply with the trial*s procedures (due for instance to medical condition likely to require an extended interruption or discontinuation) • Patients taking medications or having concomitant illnesses that are likely to influence the natural course of ADPKD (e.g. nephrotoxic medications such as chronic NSAID, cyclosporine, lithium and immunosuppressant use, and e.g. diabetes mellitus and patients with proteinuria > 1 g/24hr). • Patients, who receive renal function replacement therapy • Pregnancy at moment of inclusion • Patients with a life expectancy less than 1 year at moment of inclusion

Design outcomes

Primary

MeasureTime frame
To investigate disease progression factors and association of disease biomarkers with the onset and severity of ADPKD-related outcomes like hypertension, renal function, renal pain renal, albuminuria, renal urine concentrating ability, hematuria, cyst infection, nephrolithiasis and others.

Secondary

MeasureTime frame
To summarize the levels of self-estimated health status, pain, QoL, ADPKD-related health burden, health care resource use.

Countries

Netherlands

Contacts

Public ContactT Bais

Universitair Medisch Centrum Groningen

t.bais@umcg.nl050 361 6161

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 23, 2026