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Trial · NCT01495481

Dexmedetomidine and Adenosine: Therapeutic Use for SVT

NCT01495481, Not applicable, Completed, University of Pittsburgh; results first posted 2017-03-28

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Dexmedetomidine and Adenosine: Therapeutic Use for SVT. Trials, record NCT01495481. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01495481

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Trial

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

Title
Dexmedetomidine and Adenosine: Therapeutic Use for SVT
NCT number
NCT01495481
Status
Completed
Phases
Not applicable
Enrollment
22 participants, actual
Lead sponsor
University of Pittsburgh
Conditions
Supraventricular Tachycardia
Interventions
Dexmedetomidine, Adenosine
First posted
2011-12-20
Last updated
2017-03-28
Results first posted
2017-03-28

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryTermination of SVTWithin 3 minutesNumber of participants with SVT Termination within 3 minutes of medication administration
SecondaryNumber of Participants With Sinus Pause >2.5 Sec After Termination of SVT1 minuteEvaluation of the number of participants with sinus pause \> 2.5 sec, after dexmedetomidine vs. adenosine induced SVT termination
SecondaryNumber of Participants With Tachyarrhythmias After Medication Administration10 minutes
Number of participants with tachyarrhythmias, including Ventricular (Ventricular Tachycardia \& Fibrillation)and supraventricular (Atrial Flutter \& Fibrillation) after dexmedetomidine vs. adenosine administration
SecondaryNumber of Participants With Hypotension by Non-invasive Cuff in First 10 Minutes After Medication Administration10 minutes
Blood pressure changes after dexmedetomidine vs. adenosine. Blood pressure measured by non-invasive cuff prior to medication administration, and then at 1 min, 3 min, 5 min after medication administration. Number of participants with a significant drop in blood pressure (mmHg) compared to baseline would be counted for hypotension.

Outcomes4

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTermination of SVTWithin 3 minutesparticipantsNUMBER
SECONDARYNumber of Participants With Sinus Pause >2.5 Sec After Termination of SVT1 minuteparticipantsNUMBER
SECONDARYNumber of Participants With Tachyarrhythmias After Medication Administration10 minutesparticipantsNUMBER
SECONDARYNumber of Participants With Hypotension by Non-invasive Cuff in First 10 Minutes After Medication Administration10 minutesparticipantsNUMBER

Results by group8

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

OutcomeGroupCategoryValueSpreadUnits
Termination of SVTDexmedetomidine16participants
Termination of SVTAdenosine21participants
Number of Participants With Sinus Pause >2.5 Sec After Termination of SVTDexmedetomidine0participants
Number of Participants With Sinus Pause >2.5 Sec After Termination of SVTAdenosine16participants
Number of Participants With Tachyarrhythmias After Medication AdministrationDexmedetomidine0participants
Number of Participants With Tachyarrhythmias After Medication AdministrationAdenosine0participants
Number of Participants With Hypotension by Non-invasive Cuff in First 10 Minutes After Medication AdministrationDexmedetomidine1participants
Number of Participants With Hypotension by Non-invasive Cuff in First 10 Minutes After Medication AdministrationAdenosine0participants

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
AdenosineSTARTEDAdenosine and Dexmedetomidine22
AdenosineCOMPLETEDAdenosine and Dexmedetomidine22
AdenosineNOT COMPLETEDAdenosine and Dexmedetomidine0
WashoutSTARTEDAdenosine and Dexmedetomidine22
WashoutCOMPLETEDAdenosine and Dexmedetomidine22
WashoutNOT COMPLETEDAdenosine and Dexmedetomidine0
DexmedetomidineSTARTEDAdenosine and Dexmedetomidine22
DexmedetomidineCOMPLETEDAdenosine and Dexmedetomidine22
DexmedetomidineNOT COMPLETEDAdenosine and Dexmedetomidine0

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityDexmedetomidine
Total, all-cause mortalityAdenosine
Total, other adverse eventsDexmedetomidine022
Total, other adverse eventsAdenosine022
Total, serious adverse eventsDexmedetomidine022
Total, serious adverse eventsAdenosine022

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
18931208BACKGROUNDPubMed
21871284BACKGROUNDPubMed

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 comparisons5

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

ComparisonSource
Dexmedetomidine vs Adenosine: Number of Participants With Sinus Pause >2.5 Sec After Termination of SVTTrial comparisons
Dexmedetomidine vs Adenosine: Number of Participants With Hypotension by Non-invasive Cuff in First 10 Minutes After Medication AdministrationTrial comparisons
Dexmedetomidine vs Adenosine: Number of Participants With Tachyarrhythmias After Medication AdministrationTrial comparisons
Dexmedetomidine vs Adenosine: Termination of SVTTrial comparisons
Dexmedetomidine vs Adenosine: serious adverse eventsTrial comparisons

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/NCT01495481

GET https://conductscience.org/api/trials/v1/NCT01495481/registered