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A Rho-kinase Inhibitor (Fasudil) in the Treatment of Raynaud's Phenomenon

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Johns Hopkins University

Status and phase

Completed
Phase 3

Conditions

Scleroderma
Raynaud

Treatments

Drug: Fasudil

Study type

Interventional

Funder types

Other

Identifiers

NCT00498615
NA_00002801

Details and patient eligibility

About

Raynaud's phenomenon is thought to occur when, in response to cold or emotional stress, there is closure of the digital arteries and cutaneous arterioles leading to the clinical finding of sharp demarcated digital pallor and cyanosis of the distal skin of the fingers and/or toes. Patients often continue to experience problems despite current available treatment. The investigators' study will investigate the use of a new vasodilator called Fasudil, a Rho-kinase inhibitor. The investigators' hypothesis is that Fasudil will prevent vasoconstriction of digital and cutaneous arteries during a standard laboratory based cold exposure and will therefore improve digital blood flow and skin temperature recovery time following cold challenge. These data will provide the rationale for a more elaborate clinical trials in real life situations.

Full description

Raynaud's phenomenon (RP) is a reversible vasospastic disorder of digital arteries and cutaneous arterioles characterized by typical skin color changes and tissue ischemia (1). Avoidance of common triggers such as cold temperatures and emotional stress often leads to improvement of symptoms. When such a strategy yields inadequate benefits, pharmacologic therapy is needed.

Cutaneous vasoconstriction occurs through a general sympathetic adrenergic response and through local mechanisms in response to cold. While under normal conditions, the vasomotor tone is regulated mainly by a.2A- adrenoreceptors (a.2A-AR) expressed on vascular smooth muscle cells (VSMC) (2); during cold exposure the normally "silent" a.2C-AR relocate from the Golgi complex to the cell surface, driving the cold-induced vasoconstrictive response (3). Interestingly, the reactivity to a.2-AR stimulation is highly increased in cutaneous arteries of patients with systemic sclerosis (SSc; scleroderma) (4), and block- age of a.2C-AR has shown to shorten the time to recover digital skin temperature after a cold challenge in patients with Raynaud's Phenomenon secondary to Scleroderma (5).

The RhoA/Rho kinase pathway is activated by cooling and mediates vasoconstriction of cutaneous arteries by inducing a.2C-AR relocation to the cell surface and by increasing calcium-dependent Vascular Smooth Muscle Cells (VSMC )contractility (6). Rho kinase inhibition has been shown to effectively reduce

a.2-AR-mediated response during cold exposure and to prevent cold-induced vasoconstriction in human skin (6) Therefore, RhoA/Rho kinase inhibition may provide a highly selective intervention directed toward the mechanisms underlying thermosensitive vasomotor responses in the skin of Raynaud's Phenomenon patients.

Enrollment

17 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosis of scleroderma
  • definite Raynaud's

Exclusion criteria

  • symptomatic orthostatic hypotension
  • evidence of current malignancy
  • active ischemic digital ulcer and/or tissue gangrene
  • history of sympathectomy at any time
  • upper extremity deep vein thrombosis or lymphedema within 3 months of the study
  • recent surgical procedure requiring general anesthesia
  • current alcohol or illicit drug use
  • use of any investigational drug within 30 days of the study sessions
  • pregnancy or current breast feeding
  • subjects felt by the investigators to active disease that would affect their ability to safely participate in the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

17 participants in 3 patient groups, including a placebo group

Fasudil 80 mg
Experimental group
Description:
Subject is given a single dose of 80 mg of Fasudil ( blinded to participant and researcher) a cold challenge is given 2 hrs after the dose.
Treatment:
Drug: Fasudil
40 mg Fasudil
Experimental group
Description:
Subject is given a single dose of 40 mg of Fasudil ( blinded to participant and researcher) a cold challenge is given 2 hrs after the dose.
Treatment:
Drug: Fasudil
placebo
Placebo Comparator group
Description:
Subject is given a single dose of placebo( blinded to participant and researcher) a cold challenge is given 2 hrs after the dose.
Treatment:
Drug: Fasudil

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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