Evidence map›Paper›PMID 32398047›Full record

ArticleTrials2020

Clinical efficacy of potassium canreonate-canrenone in sinus rhythm restoration among patients with atrial fibrillation - a protocol of a pilot, randomized, double -blind, placebo-controlled study (CANREN-AF trial).

Rafał Dąbrowski, Paweł Syska, Justyna Mączyńska, Michał Farkowski, Stefan Sawicki, Agata Kubaszek-Kornatowska, Piotr Michałek, Ilona Kowalik, Hanna Szwed, Tomasz Hryniewiecki

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03536806 (Clinical Efficacy of Potassium Canrenoate - Canrenone in Sinus Rhythm Restoration Among Patients With Atrial Fibrillation and Elevated Blood Pressure - a Pilot Randomized Controlled Trial.), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03536806 phase4unknown statusnot on this map

Clinical Efficacy of Potassium Canrenoate - Canrenone in Sinus Rhythm Restoration Among Patients With Atrial Fibrillation and Elevated Blood Pressure - a Pilot Randomized Controlled Trial.

TypeinterventionalSponsorNational Institute of Cardiology, Warsaw, PolandRan2018 to 2020Enrolled80ConditionsAtrial Fibrillation, ParoxysmalArmsSaline 0.9%, Canrenone
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Rafał DąbrowskiNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland. rdabrowski@ikard.pl.
Paweł SyskaNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Justyna MączyńskaNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Michał FarkowskiNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Stefan SawickiNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Agata Kubaszek-KornatowskaNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Piotr MichałekNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Ilona KowalikNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Hanna SzwedNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Tomasz HryniewieckiNational Institute of Cardiology, ul. Alpejska 42, Warsaw, 04-628, Poland.
Institute of Cardiology · PL

Funding

National Institute of Cardiology 2.62/VII/16
6 · The paper itself

Abstract

backgroundAtrial fibrillation (AF) is the most frequent cardiac arrhythmia which increases the risk of thromboembolic complications and impairs quality of life. An important part of a therapeutic approach for AF is sinus rhythm restoration. Antiarrhythmic agents used in pharmacological cardioversion have limited efficacy and potential risk of proarrhythmia. Simultaneously, underlying conditions of AF should be treated (e.g. electrolyte imbalance, increased blood pressure, neurohormonal disturbances, atrial volume overload). There is still the need for an effective and safe approach to increase AF cardioversion efficacy. This randomized, double-blind, placebo-controlled, superiority clinical study is performed in patients with AF in order to evaluate the clinical efficacy of intravenous canrenone in sinus rhythm restoration.

methodsEighty eligible patients with an episode of AF lasting less than 48 h are randomized in a 1:1 ratio to receive canrenone or placebo. Patients randomized to a treatment intervention are receiving canrenone intravenously at a dose of 200 mg within 2-3 min. Subjects assigned to a control group obtain the same volume of 0.9% saline within the same time. The primary endpoint includes return of sinus rhythm documented in the electrocardiogram within 2 h after drug or placebo administration. Other endpoints and safety outcomes analyses, due to expected lack of statistical power, are exploratory. DISCUSSION: Current evidence supports renin-angiotensin-aldosterone system (RAAS) inhibition as an upstream therapy in AF management. Excess aldosterone secretion results in proarrhythmic effects. Among the RAAS inhibitors, only canrenone is administered intravenously. Canrenone additionally increases the plasma level of potassium, lowers blood pressure and reduces preload. It has been already used in primary and secondary hyperaldosteronism in the course of chronic liver dysfunction and in heart failure.

trial registrationClinicalTrials.gov, NCT03536806. Registered on 25 May 2018.

Indexed as

Atrial FibrillationCanrenoic AcidMineralocorticoid Receptor AntagonistsSinoatrial NodeAdministration, IntravenousAdultAgedAnti-Arrhythmia AgentsCase-Control StudiesDouble-Blind MethodElectric CountershockElectrocardiographyEquivalence Trials as TopicHeart FailureHumansMiddle AgedAnti-Arrhythmia AgentsCanrenoic AcidMineralocorticoid Receptor AntagonistsPlacebosPotassiumAtrial fibrillationCanrenoneCardioversion

Identifiers

PMID32398047
PMCPMC7218584
OpenAlexW3023996074

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.