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Vasoreactivity in Carriers of Genetic Polymorphisms

Endothelium-Dependent Vasoreactivity in Nitric Oxide Synthase Gene (Glu298Asp) Polymorphism: Studies in Healthy Volunteers

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00160888
Enrollment
100
Registered
2005-09-12
Start date
1999-11-30
Completion date
2006-12-31
Last updated
2005-09-12

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

Conditions

Healthy

Brief summary

The objective of the study is to assess the impact of genetic variation (especially polymorphisms of the gene coding endothelial nitric oxide synthase (eNOS) and the bradykinin B2 receptor gene) on venous and arterial responsiveness to vasodilators in healthy individuals without cardiovascular risk factors.

Detailed description

Study I: Using the dorsal hand vein compliance technique dose-response curves to bradykinin and sodium nitroprusside will be obtained in healthy volunteers during preconstriction with phenylephrine and after pretreatment with a single dose of 500 mg i.v. acetylsalicylic acid. Study II: Using venous occlusion plethysmography dose-response curves to acetylcholine, sodium nitroprusside and L-NG-monomethyl-arginine (L-NMMA) will be obtained in healthy volunteers pretreated with a single dose of 500mg i.v. acetylsalicylic acid.

Interventions

DRUGsodium nitroprusside, bradykinin, acetylcholine

Sponsors

Heidelberg University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
ECT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* age: 18 - 70 * gender: male * good state of health

Exclusion criteria

* known condition causing endothelial dysfunction (e.g. diabetes, hyperlipidaemia, arterial hypertension, smoking, homocysteinemia) * regular medication and/or treatment with drugs within the last 4-6 weeks (exclusion has to be decided in each case) * acute or chronic illness * methylxanthines and alcohol during 12 hours before the study * nicotine during 1 year before the study * drug and/or alcohol abuse * pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
Study I: Venous responsiveness assessed by dorsal hand vein compliance technique
Study II: Forearm blood flow assessed by venous occlusion plethysmography

Countries

Germany

Contacts

Primary ContactWalter E Haefeli, MD
Walter_Emil_Haefeli@med.uni-heidelberg.de+49-6221-56-

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026