A Rho-kinase Inhibitor (Fasudil) in the Treatment of Raynaud's Phenomenon
Primary Purpose
Raynaud, Scleroderma
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Fasudil
Sponsored by
About this trial
This is an interventional treatment trial for Raynaud focused on measuring scleroderma, Raynaud's phenomenon, Rho-kinase inhibitor
Eligibility Criteria
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.
Sites / Locations
- Johns Hopkins University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Fasudil 80 mg
40 mg Fasudil
placebo
Arm 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.
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.
Subject is given a single dose of placebo( blinded to participant and researcher) a cold challenge is given 2 hrs after the dose.
Outcomes
Primary Outcome Measures
The Time to Recover 50% of Fall in the Baseline Skin Temperature.
The time to recover 50% of the drop from baseline (prechallenge) skin temperature was derived for each subject for each cold challenge. After each of 3 study interventions received by each participant. Each participant received Fasudil 4o mg, 80 mg and placebo in a randomized sequence blinded to the participant and researchers.
Time to Recover to 70% of Fall in the Baseline Skin Temperature After Cold Challenge.
The time to recover 70% of the drop from baseline (prechallenge) skin temperature was derived for each subject for each cold challenge. After each of 3 study interventions received by each participant. Each participant received Fasudil 4o mg, 80 mg and placebo in a randomized sequence blinded to the participant and researchers.
Secondary Outcome Measures
The Blood Flow by Laser Doppler Scans of the Fingers
The measurement of the blood flow of participants prior to cold challenge 2 hours after receiving study.
Full Information
NCT ID
NCT00498615
First Posted
July 6, 2007
Last Updated
November 3, 2014
Sponsor
Johns Hopkins University
1. Study Identification
Unique Protocol Identification Number
NCT00498615
Brief Title
A Rho-kinase Inhibitor (Fasudil) in the Treatment of Raynaud's Phenomenon
Official Title
Efficacy, Tolerability and Biology of a Rho-kinase Inhibitor (Fasudil) in the Treatment of Raynaud's Phenomenon
Study Type
Interventional
2. Study Status
Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
March 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Johns Hopkins University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Raynaud, Scleroderma
Keywords
scleroderma, Raynaud's phenomenon, Rho-kinase inhibitor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Fasudil 80 mg
Arm Type
Experimental
Arm 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.
Arm Title
40 mg Fasudil
Arm Type
Experimental
Arm 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.
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
Subject is given a single dose of placebo( blinded to participant and researcher) a cold challenge is given 2 hrs after the dose.
Intervention Type
Drug
Intervention Name(s)
Fasudil
Other Intervention Name(s)
No other name found
Intervention Description
Each subject will be randomly assigned to 1 of 6 possible treatment sequences (ABC, ACB, BAC, BCA, CAB, and CBA) in a double-blind manner: A- a single oral dose of 2 placebo tablets; B- a single, oral 40 mg Fasudil dose as one 40 mg tablet and 1 placebo tablet; C- a single oral 80 mg dose as two 40 mg Fasudil tablets. Subjects will be randomized at the screening/baseline visit to a specific treatment sequence based upon a computer generated code on a 1:1:1:1:1:1 ratio for the 6 possible sequences. A single dose consisting of the two tablets will be taken after fasting for 10 hours once during each treatment period. A washout interval of at least 24 hours and no more than 7 days will be maintained between treatment periods. Concomitant medications will not be taken during the study session.
Primary Outcome Measure Information:
Title
The Time to Recover 50% of Fall in the Baseline Skin Temperature.
Description
The time to recover 50% of the drop from baseline (prechallenge) skin temperature was derived for each subject for each cold challenge. After each of 3 study interventions received by each participant. Each participant received Fasudil 4o mg, 80 mg and placebo in a randomized sequence blinded to the participant and researchers.
Time Frame
within 60 minutes
Title
Time to Recover to 70% of Fall in the Baseline Skin Temperature After Cold Challenge.
Description
The time to recover 70% of the drop from baseline (prechallenge) skin temperature was derived for each subject for each cold challenge. After each of 3 study interventions received by each participant. Each participant received Fasudil 4o mg, 80 mg and placebo in a randomized sequence blinded to the participant and researchers.
Time Frame
within 60 minutes
Secondary Outcome Measure Information:
Title
The Blood Flow by Laser Doppler Scans of the Fingers
Description
The measurement of the blood flow of participants prior to cold challenge 2 hours after receiving study.
Time Frame
Blood flow prior to cold challenge 2 hours after taking study drug
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fredrick M Wigley, M.D.
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States
12. IPD Sharing Statement
Learn more about this trial
A Rho-kinase Inhibitor (Fasudil) in the Treatment of Raynaud's Phenomenon
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