Effect of Hydroxychloroquine on Atrial Fibrillation Recurrence
Nøgleord
Abstrakt
Datoer
Sidst bekræftet: | 05/31/2018 |
Først indsendt: | 06/24/2018 |
Anslået tilmelding indsendt: | 07/17/2018 |
Først indsendt: | 07/18/2018 |
Sidste opdatering indsendt: | 07/17/2018 |
Sidste opdatering indsendt: | 07/18/2018 |
Faktisk startdato for undersøgelsen: | 07/31/2018 |
Anslået primær afslutningsdato: | 12/30/2019 |
Anslået afslutningsdato for undersøgelsen: | 07/31/2020 |
Tilstand eller sygdom
Intervention / behandling
Drug: hydrochloroquine
Fase
Armgrupper
Arm | Intervention / behandling |
---|---|
No Intervention: control receiving radiofrequency ablation and anticoagulant therapy | |
Experimental: hydrochloroquine receiving radiofrequency ablation, anticoagulant therapy and hydrochloroquine treatment (200 mg,bidpo) | Drug: hydrochloroquine 200 mg, bidpo. |
Kriterier for støtteberettigelse
Alder berettiget til undersøgelse | 18 Years Til 18 Years |
Køn, der er berettiget til undersøgelse | All |
Accepterer sunde frivillige | Ja |
Kriterier | Inclusion Criteria: - Successful radiofrequency ablation of atrial fibrillation within 24 hours Exclusion Criteria: - History of cerebrovascular disease: ischemic stroke, cerebral haemorrhage and transient ischemic attack. - History of cardiovascular disease:unstable angina, myocardial infarction, coronary revascularization and congestive heart failure. - History of renal impairment. - History of Type I diabetes mellitus or Type II diabetes uncontrolled. - History of liver impairment. - History of alcoholism or drug abuse. - Known severe skin rash or damage. - Known retinal pigmentation and visual field defect. - Allergy to any component of hydroxychloroquine. |
Resultat
Primære resultatforanstaltninger
1. Recurrence rate of atrial fibrillation after radiofrequency catheter ablation [up to 1 year]
Sekundære resultatforanstaltninger
1. Side effects [up to 1 year]