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RWD Patients With Pulmonary Arterial Hypertension Treated With IP Prostacyclin Receptor Agonists (RAMPHA)

H

Hospital Costa del Sol

Status

Enrolling

Conditions

Pulmonary Arterial Hypertension

Treatments

Drug: No intervention - Observational study

Study type

Observational

Funder types

Other

Identifiers

NCT05600218
0991-N-21

Details and patient eligibility

About

This is an observational, ambrispective study of patients in real world clinical practice, who has pulmonary arterial hypertension in whom a prostacyclin IP receptor agonist (Selexipag) is initiated between 2017 and 2021.

The aim of this study answer the following questions:

  • Changes in the mortality risk profile of these patients after treatment administration.
  • Baseline characteristics of patients initiating Selexipag.
  • Parameters used for risk stratification prior to treatment escalation.
  • Events during follow-up.

No comparison group available

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • They agree to participate in the study by signing an informed consent form

Exclusion criteria

  • Decline to participate in the study
  • Patients living 6 months or less in the reference health area
  • Patients with active malignant tumors

Trial design

60 participants in 1 patient group

Cohort 1
Description:
Patients with pulmonary arterial hypertension on treatment with prostacyclin IP receptor agonists because they are at intermediate risk of mortality at one year
Treatment:
Drug: No intervention - Observational study

Trial contacts and locations

10

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Central trial contact

Rafael Bravo Marqués, PhD, MD

Data sourced from clinicaltrials.gov

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