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Quality of Life and the Influence of Stress on the Postoperative Course of Patients After Device Implantation

U

University Hospital Essen

Status

Enrolling

Conditions

Quality of Life (QOL) and Impact of Stress

Treatments

Other: Survey using a questionnaire.

Study type

Observational

Funder types

Other

Identifiers

NCT07343466
24-12310-BO

Details and patient eligibility

About

The project "Investigating Quality of Life and the Influence of Stress on the Postoperative Course of Patients After Device Implantation" aims to investigate the relationship between stress and the postoperative healing process of patients who have had a medical device implanted. These devices include pacemakers for the treatment of bradycardia, implantable cardioverter-defibrillators (ICDs) for the treatment of tachycardia in primary and secondary prevention, and cardiac resynchronization therapy (CRT) devices and event recorders. The study will analyze the influence of stress on the postoperative course, potential complications, and overall quality of life. A combination of medical examinations and surveys will be used to analyze how psychological stress influences the physical healing process and which measures can contribute to improving quality of life and treatment success. The surgical procedure for implanting devices is not part of the study; this is an observational study.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients of legal capacity with an indication for device implantation (pacemaker, ICD, CRT, event recorder) who present at the Department of Cardiology and Angiology at the University Hospital Essen and consent to participate in the study will be included.

Exclusion criteria

  • none

Trial design

300 participants in 1 patient group

Patients with indication for device implantation (pacemaker, ICD, CRT, event recorder)
Description:
Patients with cardiac diseases, that makes a device implantation (pacemaker, ICD, CRT, event recorder) necessary, including primary and secondary indication for an ICD.
Treatment:
Other: Survey using a questionnaire.

Trial contacts and locations

1

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Central trial contact

Julia Lortz, Prof. Dr. med.; Muhammed Kurt, Dr. med.

Data sourced from clinicaltrials.gov

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