Skip to content

Rotigaptide in Endothelial Dysfunction?

Rotigaptide in Endothelial Dysfunction?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07192744
Enrollment
12
Registered
2025-09-25
Start date
2008-09-19
Completion date
2009-12-31
Last updated
2025-09-25

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

Conditions

Ischaemic Heart Diseases

Keywords

Ischaemia reperfusion, Gap junctions, Endothelial function

Brief summary

Arterial occlusion can lead to tissue ischemia and, if prolonged, end organ infarction. Clinical and experimental data would suggest that restoration of blood flow might trigger additional injury beyond that induced by the ischemia alone, so called Ischemia Reperfusion (IR) injury. IR injury impairs endothelial function through a mechanism that may involve intercellular gap junctions. Rotigaptide (ZP-123) is an anti-arrhythmic drug promoting intercellular coupling by increasing gap junction conductance. We intend to test the hypothesis that rotigaptide protects the forearm arterial circulation from IR-induced endothelial dysfunction.

Interventions

Forearm blood flow measured by venous occlusion plethysmography during interarterial infusion of vasodilators (Ach). Venous blood sampling via cannula in antecubital fossa.

Sponsors

University of Aarhus
CollaboratorOTHER
University of Oxford
CollaboratorOTHER
University of Edinburgh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy males between 18-65 years of ages, non-smokers.

Exclusion criteria

* Any concurrent illness or chronic medical condition. Concurrent use of vasoactive medication. Smoking history.

Design outcomes

Primary

MeasureTime frame
Change in forearm blood flow after ischaemia reperfusion with or without co-infusion of Rotigaptide20 fixed timepoints throughout the study up to 4 hours

Countries

United Kingdom

Outcome results

None listed

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