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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04263012
Other study ID # 2020-00017; ch19Grapow2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2019
Est. completion date December 31, 2019

Study information

Verified date February 2020
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this study is to demonstrate the challenges and the effort to set up an artificial heart program as well as to report about the follow-up treatment and the mortality rate


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 31, 2019
Est. primary completion date December 31, 2019
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who received an LVAD implant

Exclusion Criteria:

- not enough data collected

- stated will of the Patient, that his data can not be used

Study Design


Related Conditions & MeSH terms


Intervention

Other:
collection of patient data
assess mortality rate, rehospitalization and survival rate of patients after receiving an artificial heart implant

Locations

Country Name City State
Switzerland Herzchirurgie University Hospital Basel Basel

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30 days mortality mortality rate 30 days after receiving the LVAD implant 30 days after surgery
Primary rehospitalization rate rehospitalization rate of patients after receiving the LVAD implant between day of surgery and 31.12.2019
Secondary survival rate survival rate of patients after receiving the LVAD implant (Kaplan-Meier curve) between day of surgery and 31.12.2019