Page last updated: 2024-10-28

fasudil and Pain, Intractable

fasudil has been researched along with Pain, Intractable in 1 studies

fasudil: intracellular calcium antagonist; structure in first source
fasudil : An isoquinoline substituted by a (1,4-diazepan-1-yl)sulfonyl group at position 5. It is a Rho-kinase inhibitor and its hydrochloride hydrate form is approved for the treatment of cerebral vasospasm and cerebral ischemia.

Pain, Intractable: Persistent pain that is refractory to some or all forms of treatment.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Inokuchi, K1
Ito, A1
Fukumoto, Y1
Matoba, T1
Shiose, A1
Nishida, T1
Masuda, M1
Morita, S1
Shimokawa, H1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Pilot Study of Telmisartan (Micardis) For the Prevention of Acute Graft vs. Host Disease Post Allogeneic Hematopoietic Stem Cell Transplantation[NCT02338232]32 participants (Actual)Interventional2015-07-07Terminated (stopped due to Lack of Accrual)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

1 other study available for fasudil and Pain, Intractable

ArticleYear
Usefulness of fasudil, a Rho-kinase inhibitor, to treat intractable severe coronary spasm after coronary artery bypass surgery.
    Journal of cardiovascular pharmacology, 2004, Volume: 44, Issue:3

    Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Aged; Coronary Artery Bypass; Coronary Vasospasm; Dil

2004