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Trial · NCT02867878

Adenosin to Rapidly Reverse Left Ventricle Impairment in Takotsubo Syndrome

NCT02867878, Phase 2, Terminated, University Hospital of Ferrara

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Adenosin to Rapidly Reverse Left Ventricle Impairment in Takotsubo Syndrome. Trials, record NCT02867878. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02867878

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Trial

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

Title
Adenosin to Rapidly Reverse Left Ventricle Impairment in Takotsubo Syndrome
NCT number
NCT02867878
Status
Terminated
Phases
Phase 2
Enrollment
5 participants, actual
Lead sponsor
University Hospital of Ferrara
Conditions
Takotsubo Cardiomyopathy, Takotsubo Syndrome
Interventions
Adenosine, Saline solution
First posted
2016-08-16
Last updated
2018-10-23

Source ClinicalTrials.gov

Registered outcomes13

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

ListOutcomeTime frameDescription
Primaryleft ventricle ejection fraction (%)48 hoursan indipendent corelab will review all images from 48-hour ecocardiography to establish LVEF value (%)
Secondaryleft ventricle ejection fraction (%)24 hoursan indipendent corelab will review all images from 24-hour ecocardiography to establish LVEF value (%)
Secondaryleft ventricle ejection fraction (%)1 monthan indipendent corelab will review all images from 1-month ecocardiography to establish LVEF value (%)
Secondarywall motion score index24 hoursan indipendent corelab will review all images from 24-hour ecocardiography to calculate WMSI value (number)
Secondarywall motion score index48 hoursan indipendent corelab will review all images from 48-hour ecocardiography to calculate WMSI value (number)
Secondarywall motion score index1 monthan indipendent corelab will review all images from 1-month ecocardiography to calculate WMSI value (number)
Secondaryacute heart failure1 monthit is defined as dyspnea + crackles on auscultation + signs on X-ray of chest congestion
Secondaryintravenous diuretics1 monthit is defined as the total count of mg of furosemide
Secondaryemergency room admission1 monthAccess to the emergency room for dyspnea/heart failure
Secondarymajor adverse events1 yearcumulative incidence of all-cause death and hospital admission for cardiovascular causes

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.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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/NCT02867878

GET https://conductscience.org/api/trials/v1/NCT02867878/registered