Bevacizumab and Endothelium Dependent Vasodilation

Not Applicable

Completed

• Conditions: Hypertension; Cancer; Endothelial Dysfunction
• Interventions: Drug: Acetylcholine; Drug: Nitroprusside; Drug: Bevacizumab

• Registration Number: NCT01125943
• Lead Sponsor: Radboud University Medical Center

Brief Summary

The introduction of angiogenesis inhibitors has remarkably improved treatment of patients with several types of cancer. One of the most reported side effects of angiogenesis inhibitors is hypertension. In patients treated with bevacizumab, a monoclonal antibody against vascular endothelial growth factor, hypertension had an overall incidence up to 32%. The increase in blood pressure occurs early in treatment. The etiology of hypertension caused by treatment with angiogenesis inhibitors is unclear. Understanding the pathogenesis of this side effect is essential for optimal treatment with this class of drugs.

The primary objective is to explore the effect of bevacizumab infusion on endothelium-dependent vasodilation of forearm resistance arteries.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2010-05-17
• Study First Submitted QC: 2010-05-17
• Study First Posted: 2010-05-19
• Study Start: 2010-06
• Primary Completion: 2011-10
• Study Completion: 2011-11
• Status Verified: 2013-01
• Last Update Submitted: 2013-01-08
• Last Update Posted: 2013-01-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 24

Inclusion Criteria

1. Age 18-50 years 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

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. First degree relatives with a history of premature cardiovascular disease before the age of 50
6. Current use of medication.
7. Clinical evidence of cardiac or pulmonary disease
8. Hypertension ( systole >140mmHG, diastole >90mmHg)
9. Diabetes mellitus
10. Smoking
11. Any clinically relevant abnormality on ECG.
12. A history of thrombosis or first degree family members with a history of recurrent thrombosis
13. Inability to understand the nature and extent of the trial and the procedures required.
14. Previous participation in a study with bevacizumab

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Nitroprusside	Bevacizumab	Infusion of two increasing dosages of nitroprusside during 5 minutes each during the continuous infusion of bevacizumab
Acetylcholine	Acetylcholine	Intra-arterial infusion of acetylcholine in two increasing dosages during 5 minutes each during the intra-arterial infusion of bevacizumab
Acetylcholine	Bevacizumab	Intra-arterial infusion of acetylcholine in two increasing dosages during 5 minutes each during the intra-arterial infusion of bevacizumab
Nitroprusside	Nitroprusside	Infusion of two increasing dosages of nitroprusside during 5 minutes each during the continuous infusion of bevacizumab

Primary Outcome Measures

Name	Time	Method
Vasomotor response assessed by venous occlusion strain gauge plethysmography	15 minutes	Response to infusion of bevacizumab and/or acetylcholin or nitroprusside

Trial Locations

Locations (1)

Radboud University Nijmegen Medical Centre; 🇳🇱 Nijmegen, Netherlands