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Recruiting NCT07051967

NCT07051967 Post-intensive Care Syndromes in Pregnant Patients With Respiratory Failure and COVID-19 Compared to Non-pregnant Patients With Respiratory Failure and COVID-19

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Clinical Trial Summary
NCT ID NCT07051967
Status Recruiting
Phase
Sponsor Charite University, Berlin, Germany
Condition COVID-19
Study Type OBSERVATIONAL
Enrollment 40 participants
Start Date 2025-09-22
Primary Completion 2026-06-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

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 40 participants in total. It began in 2025-09-22 with a primary completion date of 2026-06-30.

⚠ 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 characterize patients in the Post-Intensive-Care-Syndrome (PICS) outpatient clinic based on routine data and to evaluate their treatment outcome over the course of their treatment. For this purpose, data sets from approx. 40 patients who were treated in the intensive care unit subsequently evaluated in the PICS outpatient clinic between March 27, 2020, and May 6, 2024, will be analyzed.

Eligibility Criteria

Inclusion Criteria: * Age: 18 years and older * Admission to a Charité intensive care unit and follow-up examination by the Post-Intensive-Care-Syndrome (PICS) outpatient clinic of the Department of Anesthesiology and Intensive Care Medicine between March 27, 2020 and May 6, 2024. * COVID-19 infection in temporal assocoation with the intensive care unit admission. * Intensive care unit admission with lung failure or development of lung failure in the course of intensive care unit treatment. * Admission to the intensive care unit with lung failure or development of lung failure during intensive care unit stay. Exclusion Criteria: * Gender: Male * Diagnosis: Non-COVID or no respiratory failure

Contact & Investigator

Central Contact

Claudia Spies, MD Prof.

✉ claudia.spies@charite.de

📞 +49 30 450 551102

Principal Investigator

Claudia Spies, MD, Prof.

STUDY DIRECTOR

Charite University, Berlin, Germany

Frequently Asked Questions

Who can join the NCT07051967 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying COVID-19. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07051967 currently recruiting?

Yes, NCT07051967 is actively recruiting participants. Contact the research team at claudia.spies@charite.de for enrollment information.

Where is the NCT07051967 trial being conducted?

This trial is being conducted at Berlin, Germany.

Who is sponsoring the NCT07051967 clinical trial?

NCT07051967 is sponsored by Charite University, Berlin, Germany. The principal investigator is Claudia Spies, MD, Prof. at Charite University, Berlin, Germany. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology