The "Seamless" Patient:From Preoperative Preparation to Postoperative Rehabilitation
Recruiting · NCT06699446 · Interventional (participants receive a specific treatment) · Lead sponsor: Hannover Medical School
View the official record on ClinicalTrials.gov →Interventions studied
pre rehabilitation
What this trial is about
The "seamless" patient: from preoperative preparation to postoperative rehabilitation. The effects of digital services for perioperative care of patients undergoing cardiac surgery will be investigated
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Patient is capable of giving consent;
- planned, elective cardiac surgery (coronary bypass surgery and heart valve surgery incl. combination surgery). The planned surgery can be performed with or without a heart-lung machine.
- Minimally invasive procedures may also be explicitly included in the study.
Exclusion criteria
- Emergency care;
- congenital heart defects;
- age less than 18 years;
- patient unable to give consent;
- patient unable to perform simple physical training;
- high-risk surgery with a calculated Euroscore II of more than 8%.
Where it is running
1 location listed.
- Medical School Hanover - Hanover, Lower Saxony, Germany