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Primary graft dysfunction after cardiac Transplantation: a prospective study on incidence, outcome and risk factors

Primary graft dysfunction after cardiac Transplantation: a prospective study on incidence, outcome and risk factors - PGD-Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021454
Enrollment
200
Registered
2020-12-02
Start date
2019-02-27
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

PGD after HTX

Interventions

Group 1: 200 patients are to be included over a period of 2,5 years. The study will last 5 years in total. Study protocol: From every patient in our institution, undergoing cardiac transplantation for

Sponsors

Herz- u. Diabeteszentrum NRW Klinik für Thorax- u. Kardiovaskularchirurgie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who have had a heart transplantation for the first time

Exclusion criteria

Exclusion criteria: Patients who have already had an allograft transplantation. Patients incapable of giving consent.

Design outcomes

Primary

MeasureTime frame
The occurrence of primary graft dysfunction after heart transplantation according to the ISHLT criteria.

Secondary

MeasureTime frame
In-hospital mortality, 30-day mortality, morbidity (apoplex, bleeding, GIT complications, liver and renal failure), infections / sepsis, rejection episodes, 1-year survival, re-thoracotomy

Countries

Germany

Contacts

Public ContactHeike Windhagen

Herz- u. Diabeteszentrum NRW Klinik für Thorax- u. Kardiovaskularchirurgie Studienabteilung Chirurgie

hwindhagen@hdz-nrw.de+49-5731-97-3135

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026