NCT05789953 PrEventing PostoPERative Pulmonary Complications by Establishing a MachINe-learning assisTed Approach
| NCT ID | NCT05789953 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Britta Trautwein |
| Condition | Postoperative Pulmonary Complications |
| Study Type | OBSERVATIONAL |
| Enrollment | 512 participants |
| Start Date | 2023-04-25 |
| Primary Completion | 2026-09 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
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 512 participants in total. It began in 2023-04-25 with a primary completion date of 2026-09.
⚠ 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
Postoperative pulmonary complications (POPC) are common after general anaesthesia and are a major cause of increased morbidity and mortality in surgical patients. However, prevention and treatment methods for POPC that are considered effective, tie up human and technical resources. The aim of the planned research project is therefore to enable reliable identification of high-risk patients on the basis of a tailored machine learning algorithm using perioperative clinical routine data and sonographic imaging data collected in the recovery room. The randomized clinical trial will include 512 patients undergoing elective surgery in general anaesthesia. The primary outcome will be the development of POPC. The goal of the study is to detect postoperative pulmonary complications before they become clinically manifest.
Eligibility Criteria
Inclusion Criteria: * adult patients * elective, surgical procedure * general anaesthesia Exclusion Criteria: * patients younger than 18 years of age * outpatient surgery * postoperative admission to intensive care unit
Contact & Investigator
Frequently Asked Questions
Who can join the NCT05789953 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Postoperative Pulmonary Complications. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05789953 currently recruiting?
Yes, NCT05789953 is actively recruiting participants. Contact the research team at britta.trautwein@uniklinik-ulm.de for enrollment information.
Where is the NCT05789953 trial being conducted?
This trial is being conducted at Ulm, Germany.
Who is sponsoring the NCT05789953 clinical trial?
NCT05789953 is sponsored by Britta Trautwein. The trial plans to enroll 512 participants.