The PSVT Place Registry.Paroxysmal Supraventricular Tachycardia (PSVT) Registry.
Stopped early
Conditions studied: Paroxysmal Supraventricular Tachycardia (PSVT)
In brief
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.
Key facts
- Study ID
- NCT03353610
- Run by
- Milestone Pharmaceuticals Inc.
- People needed
- 354
- Starts
- 2017-10-16
- Expected to finish
- 2020-03-16
- Last updated by the study team
- 2020-12-03
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- A participant must meet all of the following criteria to be eligible for participation in the study:
- Adult male or female.
- Participant has suspected PSVT as per the online prescreening assessment.
- Participant lives in a country in which the registry is being conducted.
- Participant has signed the informed consent form indicating he/she is able to complete the online registry data collection forms on his/her own.
You may not qualify if…
- Participant does not have an email address.
- Participant does not set up a user account.
Where it is running
- MAPI — Lexington, Kentucky, United States
Full record on ClinicalTrials.gov
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