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Markers for Acute Chemotherapy induced Cardiovascular changes.

Evaluation of markers for cardiovascular changes during and after cisplatin based chemotherapy in patients with testicular cancer.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28599
Enrollment
50
Registered
2006-05-19
Start date
2006-05-16
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

testicular cancer

Interventions

The number of circulating endothelial cells, endothelial marker proteins and accumulation of AGEs (estimated by measuring skin autofluorescence with an AGE-reader) will be determined before, during an

Sponsors

Department of Internal Medicine: Division of Medical Oncology, University Medical Center Groningen (UMCG)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with disseminated testicular cancer who will be treated with cisplatin based chemotherapy; 2. Age 18-50 years at start of treatment; 3. Written informed consent.

Exclusion criteria

Exclusion criteria: 1. Medical history of cardiovascular disease; 2. Known renal disease or estimated glomerular filtration rate (GFR) < 60 ml/min (using Cockcroft-Gault formula).

Design outcomes

Primary

MeasureTime frame
The early effects of cisplatin based chemotherapy on the number of circulating endothelial (progenitor) cells and the accumulation of AGEs, and their correlation with cardiovascular damage.

Secondary

MeasureTime frame
1. Evaluation of which treatment and patient related factors (for example chemotherapy dose and presence of cardiovascular risk factors) predispose to cardiovascular damage during and after cisplatin based chemotherapy; 2. Determination of circulating apoptosis markers during and after cisplatin based chemotherapy and their relation to tumor response and cardiovascular damage.

Contacts

Public ContactE.C. Haas de

Medische Oncologie, Universitair Medisch Centrum Groningen, Hanzeplein 1

e.c.de.haas@int.umcg.nl+31 (0)50 3612821

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)