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NCT03353610

The PSVT Place Registry.Paroxysmal Supraventricular Tachycardia (PSVT) Registry.

Terminated Last updated 3 December 2020
What this trial tests

trial in Paroxysmal Supraventricular Tachycardia (PSVT) in 354 participants. Terminated before completion.

Timeline
16 October 2017
Primary endpoint
16 March 2020
16 March 2020

Quick facts

Lead sponsorMilestone Pharmaceuticals Inc.
StatusTerminated
Study typeOBSERVATIONAL
Enrollment354
Start date16 October 2017
Primary completion16 March 2020
Estimated completion16 March 2020
Sites1 location across United States

Conditions studied

Sponsor

Milestone Pharmaceuticals Inc. — full company profile →

Who can join

Eligibility, any sex, with Paroxysmal Supraventricular Tachycardia (PSVT). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Paroxysmal supraventricular tachycardia (PSVT) is a sporadic, sudden, and recurring tachycardia that is caused by an altered electrical conductivity in the heart. It causes palpitations and a rapid heart rate, which may induce fear in the patient and negatively impact the patient's quality of life. Therefore, most patients experience not only physical symptoms of PSVT, but also dramatic psychological burdens. As PSVT drug development efforts advance, it has become increasingly important to document the impact of PSVT in a systematic way, in terms of the disease natural history and clinical characteristics of PSVT episodes, as well as the psychological impact of the condition as reported by patients over time. In order to meet the needs for ongoing, systematic data collection on PSVT, a multinational registry, The PSVT Place Registry (www.PSVTPlaceRegistry.com), is being implemented and will be initially comprised of data entered directly by patients. The long-term registry is designed with a participant-focused approach to enable continuity of data collection and minimization of impact from changes of participants' health care providers. The registry may be expanded at a later time to include physician-reported data. The information from the registry is planned to be a resource for participants with PSVT, their families and support networks, their doctors, and the research community to better understand PSVT-related symptoms and awareness, PSVT diagnoses, patient self-management, medical treatments for PSVT, and impact of PSVT on quality of life from the patient perspective.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03353610.

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