Skip to content

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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07051967
Enrollment
40
Registered
2025-07-04
Start date
2025-09-22
Completion date
2026-06-30
Last updated
2025-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome Due to COVID-19, COVID-19, Pregnancy Related

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.

Detailed description

This is a retrospective comparison of approximately 13 pregnant patients and approximately 27 non-pregnant patients who developed respiratory failure (also known as acute respiratory distress syndrome, or ARDS) due to COVID-19 infection. The analysis is based on routine treatment data from the Post-Intensive Care Syndrome (PICS) outpatient clinic of the Department of Anesthesiology and Intensive Care Medicine (CCM/CVK), as well as intensive care treatment data, primarily from the Department of Anesthesiology and Intensive Care Medicine (CCM/CVK). In some cases, additional data were obtained from the Medical Clinic for Nephrology and Internal Intensive Care Medicine (CCM/CVK/CBF), the Medical Clinic specializing in Hepatology and Gastroenterology (CCM/CVK), and the Department of Infectiology, Pulmonology, and Intensive Care Medicine (CCM).

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Impairment in at least one PICS domain (mobility, cognition, and/or mental health)27.03.2020-06.05.2024Impairment in at least one PICS domain (mobility, cognition, and/or mental health) after discharge from the ICU, assessed at the time of presentation to the PICS outpatient clinic. The planned PICS outpatient presentation takes place 3 and 6 months (ranging from 1 month to 3 years) after the initial ICU stay.

Secondary

MeasureTime frameDescription
Catecholamine therapy27.03.2020-06.05.2024Catecholamine therapy during intensive care unit (ICU) treatment is measured in doses and duration.
Extracorporeal Membrane Oxygenation treatment27.03.2020-06.05.2024Extracorporeal Membrane Oxygenation treatment in the ICU Yes or No
Need for ventilation during ICU treatment27.03.2020-06.05.2024Need for ventilation during ICU treatment and, if so, ventilation route (non-invasive and invasive, endotracheal tube and tracheostomy tube) and duration of ventilation
Duration of ventilation during ICU treatment27.03.2020-06.05.2024Duration of ventilation during ICU treatment is measured in hours
Oxygenation index27.03.2020-06.05.2024Oxygenation index/Horowitz index is defined as the ratio of the arterial partial pressure of oxygen (PaO₂, in mmHg) to the fraction of inspired oxygen (FiO₂, expressed as a decimal).
Severity of illness27.03.2020-06.05.2024Severity of illness during ICU treatment is assessed with validated intensive care unit scores.
Incidence of delirium27.03.2020-06.05.2024Incidence of delirium in the ICU is measured with validated delirium scores.
Duration of delirium27.03.2020-06.05.2024Duration of delirium in the ICU is measured in days
Sedation Medications27.03.2020-06.05.2024Kind of medications required for sedation.
Sedation dosage27.03.2020-06.05.2024The amount of drug required for sedation.
Duration of sedation27.03.2020-06.05.2024Duration of sedation is measured in days.
Continuous muscle relaxation27.03.2020-06.05.2024Continuous muscle relaxation during ICU treatment
Vaccination status27.03.2020-06.05.2024Vaccination status at the start of ICU treatment
COVID-19-specific immunotherapy27.03.2020-06.05.2024COVID-19-specific immunotherapy (e.g., tocilizumab, dexamethasone, baricitinib) during ICU treatment
Type of Anti-infective therapy27.03.2020-06.05.2024Type of anti-infective therapy during ICU treatment
Duration of Anti-infective therapy27.03.2020-06.05.2024Duration of anti-infective therapy during ICU treatment is measured in days.
Week of pregnancy27.03.2020-06.05.2024Week of pregnancy during ICU treatment in the pregnant women group
Need for a cesarean section27.03.2020-06.05.2024Need for a cesarean section in the pregnant women group, yes or no.
Depth of sedation27.03.2020-06.05.2024Depth of sedation during ICU treatment
Nutrition27.03.2020-06.05.2024Nutrition (enteral vs. parenteral) during ICU treatment
Dialysis 127.03.2020-06.05.2024Dialysis during ICU treatment (binary)
Dialysis 227.03.2020-06.05.2024Dialysis during ICU treatment (duration)
Intensive care unit mortality27.03.2020-06.05.2024Data from patient records
Hospital mortality27.03.2020-06.05.2024Data from patient records
90-day mortality27.03.2020-06.05.2024Data from patient records
180-day mortality27.03.2020-06.05.2024Data from patient records
Intensive care unit length of stay27.03.2020-06.05.2024Participants are followed up for the duration of intensive care unit stay, an expected average of 2 days
Duration of Hospital stay27.03.2020-06.05.2024Participants are followed up for the duration of hospital stay, an expected average of 7 days
Grip strength Test27.03.2020-06.05.2024Grip strength at the time of presentation to the PICS outpatient clinic is measured with a dynamometer.
Mobility27.03.2020-06.05.2024Mobility at the time of presentation to the PICS outpatient clinic is measured with the Timed Up-and-Go (TUG).
Cognition 127.03.2020-06.05.2024Cognition 1 at the time of presentation to the PICS outpatient clinic is measured with the MiniCog. The MiniCog consists of two items, the word recall test and the clock-drawing test. Performance in these test is rated on a scale ranging from 0 - 5, with \<3 points indicating a suspicion of dementia.
Cognition 227.03.2020-06.05.2024Cognition 2 at the time of presentation to the PICS outpatient clinic is measured with the Animal Naming Test
Mental health27.03.2020-06.05.2024Mental health at the time of presentation to the PICS outpatient clinic is measured with Patient Health Questionnaire-4 (It comprises the first two questions of the depression module of the PHQ-D \[PHQ-2\] and the first two questions of the module for assessing generalized anxiety \[GAD-2\]) and patient questionnaire with subjective patient assessment.
PBQ Parent-Child Relationship Questionnaire27.03.2020-06.05.2024PBQ at the time of presentation to the PICS outpatient clinic. This questionnaire is a 25-question self-completion questionnaire, which was developed in order to recognize disorders in the mother-child relationship at an early stage. The questionnaire is made up of 4 scales. Scale 1 Delayed attachment cut-off 12, Scale 2 Rejection and anger cut-off 17, Scale 3 Anxiety cut-off 10 and Scale 4 Risk of child abuse cut-off 3.
Edinburgh Postpartum Depression Questionnaire (EPDS)27.03.2020-06.05.2024The Edinburgh Postnatal Depression Scale (EDPS) was developed to identify women who may have postpartum depression. Each answer is given a score of 0 to 3 .The maximum score is 30. A score of more than 10 suggests minor or major depression may be present.
Health-related quality of life27.03.2020-06.05.2024Health-related quality of life at the time of presentation to the PICS outpatient clinic is measured with EQ-5D-5L questionnaire. Higher Score indicate better Healt-related quality of life.
Organ complications27.03.2020-06.05.2024Organ complications, including bleeding and pregnancy complications during hospital treatment. Data from patient records.

Countries

Germany

Contacts

Primary ContactClaudia Spies, MD Prof.
claudia.spies@charite.de+49 30 450 551102

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026