ConductScience.org, home

Trial · NCT02248753

Acute Cardioversion Versus Wait And See-approach for Symptomatic Atrial Fibrillation in the Emergency Department

NCT02248753, Not applicable, Completed, Maastricht University Medical Center

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. Acute Cardioversion Versus Wait And See-approach for Symptomatic Atrial Fibrillation in the Emergency Department. Trials, record NCT02248753. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02248753

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Acute Cardioversion Versus Wait And See-approach for Symptomatic Atrial Fibrillation in the Emergency Department
NCT number
NCT02248753
Status
Completed
Phases
Not applicable
Enrollment
437 participants, actual
Lead sponsor
Maastricht University Medical Center
Conditions
Atrial Fibrillation
Interventions
Pharmacological cardioversion - Flecainide, Electrical cardioversion, Metoprolol, Verapamil, Digoxin, Pharmacological cardioversion - Amiodarone
First posted
2014-09-25
Last updated
2020-01-21

Source ClinicalTrials.gov

Registered outcomes7

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primary12-lead ECG4 weeksPresence of sinus rhythm on ECG
SecondaryTime to conversion to sinus rhythm (Holter monitor)48 hoursIntervention group only
SecondaryQuality of life (SF-36)Baseline, 4 weeks, 6 months, 12 months
SecondaryOne-year follow-up of Major Adverse Cerebrovascular or Cardiovascular EventsOne year
SecondaryTime to first recurrence of Atrial Fibrillation1 monthMonitoring through handheld device
SecondaryTotal health care and societal costs1 year
SecondaryQuality of Life (AFEQT)Baseline, 4 weeks, 6 months, 12 months

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers3

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
27979041BACKGROUNDPubMed
30883054DERIVEDPubMed
36322782DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02248753

GET https://conductscience.org/api/trials/v1/NCT02248753/registered