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Bevacizumab and vasoconstriction

Bevacizumab and vasoconstriction - Bevacizumab and vasoconstriction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON33520
Enrollment
10
Registered
2009-03-25
Start date
2009-06-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

elevated blood pressure Hypertensie

Interventions

Intra-arterial infusion of bevacizumab

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-50years old 2. Male 3. Results of serum glucose, lipids and creatinine should be within the laboratory's reference ranges. 4. Subject is able and willing to sign the Informed Consent Form prior to screening evaluations.

Exclusion criteria

Exclusion criteria: 1. Documented history of sensitivity/idiosyncrasy to medicinal products or excipients. 2. History of or current abuse of drugs, alcohol or solvents. 3. History of malignant disease. 4. First degree relatives with a history of cancer before the age of 50 5. Current use of medication. 6. Clinical evidence of cardiac or pulmonary disease 7. Hypertension ( systole >140mmHG, diastole >90mmHg) 8. Diabetes mellitus 9. Smoking 10. Any clinically relevant abnormality on ECG. 11. Inability to understand the nature and extent of the trial and the procedures required.

Design outcomes

Primary

MeasureTime frame
The fore-arm vasomotor response to administered bevacizumab, expressed as percentage change in forerarm blood flow ratio ( flow infused arm flow control arm form baseline

Secondary

MeasureTime frame
Correlation between VEGF concentrations in plasma and the vasoconstrictive response to bevacizumab

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)