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RWD Patients With Pulmonary Arterial Hypertension Treated With IP Prostacyclin Receptor Agonists

Real World Andalusian Multicenter Data on Patients With Pulmonary Arterial Hypertension Treated With IP Prostacyclin Receptor Agonists

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05600218
Acronym
RAMPHA
Enrollment
60
Registered
2022-10-31
Start date
2021-06-01
Completion date
2024-12-31
Last updated
2022-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Arterial Hypertension

Keywords

Pulmonary Arterial Hypertension, Selexipag, Real World Data, Effectiveness

Brief summary

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

Interventions

Real life drug evaluation

Sponsors

Hospital Universitario Virgen Macarena
CollaboratorOTHER
Hospital Regional de Malaga
CollaboratorOTHER
Hospital Universitario Virgen de la Victoria
CollaboratorOTHER
Hospital San Juan de la Cruz
CollaboratorOTHER
Complejo Hospitalario de Especialidades Juan Ramón Jimenez
CollaboratorOTHER
Hospitales Universitarios Virgen del Rocío
CollaboratorOTHER
Hospital Clinico Universitario San Cecilio
CollaboratorOTHER
Hospital Universitario de Valme
CollaboratorOTHER
Hospital de Poniente
CollaboratorUNKNOWN
Hospital Costa del Sol
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Clinical improvement (risk profile)12 monthsPercentage of patients reducing annual mortality risk profile according to ESC/ERS Clinical Practice Guidelines 2015 Risk Stratification.

Secondary

MeasureTime frameDescription
Risk stratification variablesBasalinePercentage of clinical tests that have been used to include study treatment.
Events12 monthsIncidence of events in follow-up: admission for worsening pulmonary hypertension; need for systemic prostacyclins; unscheduled admission for any cause; death related to pulmonary hypertension; death from any cause.

Countries

Spain

Contacts

Primary ContactRafael Bravo Marqués, PhD, MD
rafabravomarques@gmail.com034 686202746

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026