NCT06175650 Towards a Sex-specific "Female Enhanced Recovery After Cardiac Surgery'' (F-ERAS) Pathway:
| NCT ID | NCT06175650 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Jennifer Breel |
| Condition | Female |
| Study Type | OBSERVATIONAL |
| Enrollment | 5,500 participants |
| Start Date | 2023-11-21 |
| Primary Completion | 2025-11-21 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 5,500 participants in total. It began in 2023-11-21 with a primary completion date of 2025-11-21.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of this study is to evaluate the differences between men and women undergoing cardiac surgery. We will look at perioperative factors such as body weight, body surface area, previous medical history, pharmacokinetics, transfusion, coagulation, cardiopulmonary bypass (CPB) related factors, cardiac function, inotropic requirements, risk, and outcome scores as well as morbidity and mortality at 30 and 90 days, 1, 5, and 10 years.
Eligibility Criteria
Inclusion Criteria: * Patients \> 18 years * All patients who underwent cardiac surgery from 1 January 2016 to the start of the study, in either of the centres (AMC or VUmc) (retrospective) * All patients undergoing cardiac surgery from the start of the study (\~March 2022) until approximately 2032 Exclusion Criteria: • Patients who object to the re-use of their care data or do not give consent
Contact & Investigator
Markus W Hollmann, Professor
PRINCIPAL INVESTIGATOR
Anesthesiology and Pain Medicine, Amsterdam Medical Center
Frequently Asked Questions
Who can join the NCT06175650 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Female. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06175650 currently recruiting?
Yes, NCT06175650 is actively recruiting participants. Contact the research team at j.s.breel@amsterdamumc.nl for enrollment information.
Where is the NCT06175650 trial being conducted?
This trial is being conducted at Amsterdam, Netherlands.
Who is sponsoring the NCT06175650 clinical trial?
NCT06175650 is sponsored by Jennifer Breel. The principal investigator is Markus W Hollmann, Professor at Anesthesiology and Pain Medicine, Amsterdam Medical Center. The trial plans to enroll 5,500 participants.