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D013617: Tachycardia, Supraventricular

Developed by Shray Alag, The Harker School
Sections: Correlations, Clinical Trials, and HPO

Correlations computed by analyzing all clinical trials.

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Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug1549 Etripamil Wiki 1.00
drug3195 Placebo Wiki 0.04

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D013610 Tachycardia NIH 0.58

Correlated HPO Terms (2)


Name (Synonyms) Correlation
HP:0004755 Supraventricular tachycardia HPO 1.00
HP:0001649 Tachycardia HPO 0.58

Clinical Trials

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There is one clinical trial.


1 Multi-Centre, Randomized, Double-Blind, Placebo-Controlled, Efficacy, and Safety Study of Etripamil Nasal Spray for the Termination of Spontaneous Episodes of Paroxysmal Supraventricular Tachycardia. NODE 301 Trial.

This is a two-part, multi-center, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of etripamil NS self-administered by patients who experience an episode of paroxysmal ventricular tachycardia (PSVT) in an at-home setting. Part 1 comprised the conduct of the NODE-301 study up to the date of the adjudication of 150th positively adjudicated PSVT episode and Part 2 comprises the conduct of the NODE-301 study after the completion of Part 1. The RAPID Study (NODE-301 - Part 2) will enroll patients enrolled during Part 1 who had not dosed with the double-blind study drug, or had not discontinued the study before the adjudication of the 150th positively adjudicated PSVT episode in Part 1, and patients enrolled into the study following the completion of Part 1. Enrollment will continue until and for approximately 6 months after the date of the adjudication of the 180th positively adjudicated PSVT episode. The study will include the following visits: A Screening Visit, A Test Dose Randomization Visit, Monthly Follow-up Visits, A Randomized Treatment Period, A Randomized Treatment Period Follow-Up Visit, An Open-Label Treatment Period, and A Final Study Visit.

NCT03464019
Conditions
  1. Paroxysmal Supraventricular Tachycardia
Interventions
  1. Drug: Etripamil
  2. Drug: Placebo
MeSH:Tachycardia Tachycardia, Supraventricular
HPO:Supraventricular tachycardia Tachycardia

Primary Outcomes

Description: The primary efficacy endpoint is defined as an adjudicated termination of a positively adjudicated episode of PSVT (AV nodal reentrant tachycardia or AV reentrant tachycardia determination if possible) and conversion to sinus rhythm (SR) for at least 30 seconds within 30 minutes of start of study drug dosing.

Measure: The time to conversion of an episode of PSVT to sinus rhythm (SR) after study drug administration.

Time: Within 30 minutes of start of study drug dosing.

Secondary Outcomes

Measure: Relief of specific symptoms (i.e., heart palpitations, rapid pulse feeling, chest pain, anxiety, shortness of breath, dizziness, and fainting) potentially associated with an episode of PSVT.

Time: 5 hours after administration of study drug

Measure: Rating of Treatment Satisfaction Questionnaire for Medication (TSQM).

Time: 5 hours after administration of study drug

Other Outcomes

Measure: The number of positively adjudicated episodes of PSVT terminated by a vagal maneuver (VM).

Time: Up to 2 years

Measure: The percentage of patients requiring additional medical intervention to terminate an episode of PSVT.

Time: 5 hours after administration of study drug

Measure: The repeat of key efficacy endpoints in various subgroups of interest (e.g., concomitant medications).

Time: 5 hours after administration of study drug

HPO Nodes


Reports

Data processed on December 13, 2020.

An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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