Page last updated: 2024-11-05

tranexamic acid and Orphan Diseases

tranexamic acid has been researched along with Orphan Diseases in 2 studies

Tranexamic Acid: Antifibrinolytic hemostatic used in severe hemorrhage.

Orphan Diseases: Rare diseases that have not been well studied.

Research Excerpts

ExcerptRelevanceReference
"Tranexamic acid (TA) has been widely used in the treatment of these severe bleeds but with no properly designed trial."6.79Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross-over controlled trial in a rare disease. ( Boutitie, F; Capitaine, AL; Dupuis-Girod, S; Gaillard, S; Gueyffier, F; Hatron, PY; Kaminsky, P; Manfredi, G; Morinière, S; Plauchu, H; Rivière, S; Roy, P, 2014)
"Tranexamic acid (TA) has been widely used in the treatment of these severe bleeds but with no properly designed trial."2.79Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross-over controlled trial in a rare disease. ( Boutitie, F; Capitaine, AL; Dupuis-Girod, S; Gaillard, S; Gueyffier, F; Hatron, PY; Kaminsky, P; Manfredi, G; Morinière, S; Plauchu, H; Rivière, S; Roy, P, 2014)
"Glanzmann thrombasthenia (GT) is a rare bleeding syndrome, which is characterized by a lack of platelet aggregation."1.36Glanzmann thrombasthenia detected because of knee hemarthrosis: a case report. ( Ishiguro, N; Katsumi, A; Nishida, Y; Tsukushi, S; Urakawa, H, 2010)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gaillard, S1
Dupuis-Girod, S1
Boutitie, F1
Rivière, S1
Morinière, S1
Hatron, PY1
Manfredi, G1
Kaminsky, P1
Capitaine, AL1
Roy, P1
Gueyffier, F1
Plauchu, H1
Urakawa, H1
Nishida, Y1
Tsukushi, S1
Katsumi, A1
Ishiguro, N1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Tranexamic Acid to Prevent OpeRation in Chronic Subdural Hematoma. A Double-blind, Placebo-controlled, Multicentre, Randomized Controlled Clinical Trial[NCT03582293]Phase 3140 participants (Anticipated)Interventional2018-06-19Recruiting
ATERO : A Randomised Study With Tranexamic Acid in Epistaxis of Rendu Osler Syndrome. Beneficial or Iatrogenic Effects.[NCT00355108]Phase 3170 participants (Actual)Interventional2006-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trials

1 trial available for tranexamic acid and Orphan Diseases

ArticleYear
Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross-over controlled trial in a rare disease.
    Journal of thrombosis and haemostasis : JTH, 2014, Volume: 12, Issue:9

    Topics: Adult; Aged; Antifibrinolytic Agents; Cross-Over Studies; Double-Blind Method; Epistaxis; Europe; Fe

2014
Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross-over controlled trial in a rare disease.
    Journal of thrombosis and haemostasis : JTH, 2014, Volume: 12, Issue:9

    Topics: Adult; Aged; Antifibrinolytic Agents; Cross-Over Studies; Double-Blind Method; Epistaxis; Europe; Fe

2014
Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross-over controlled trial in a rare disease.
    Journal of thrombosis and haemostasis : JTH, 2014, Volume: 12, Issue:9

    Topics: Adult; Aged; Antifibrinolytic Agents; Cross-Over Studies; Double-Blind Method; Epistaxis; Europe; Fe

2014
Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross-over controlled trial in a rare disease.
    Journal of thrombosis and haemostasis : JTH, 2014, Volume: 12, Issue:9

    Topics: Adult; Aged; Antifibrinolytic Agents; Cross-Over Studies; Double-Blind Method; Epistaxis; Europe; Fe

2014

Other Studies

1 other study available for tranexamic acid and Orphan Diseases

ArticleYear
Glanzmann thrombasthenia detected because of knee hemarthrosis: a case report.
    Journal of pediatric orthopedics. Part B, 2010, Volume: 19, Issue:6

    Topics: Antifibrinolytic Agents; Arthralgia; Bleeding Time; Child; Diagnosis, Differential; Hemarthrosis; Hu

2010