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NCT06728709Completed

Lung Ultrasound in Critically Ill Obstetrics and Gynecological Patients

Perioperative Lung Ultrasound Phenotypes and Clinical Outcomes in Critically Ill Obstetrics and Gynaecologic Patients (POLUS): A Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 14 Jul 2026

Brief summary (registry, in English)

Pulmonary dysfunction aggravates the illness of critically ill obstetrics and gynecological patients. Early identification with bedside technique and prompt management may improve the outcome of critical care in this vulnerable population

Status (registry)
Completed
Study type
Observational
Enrollment
280 (actual)
First submitted
1 Aug 2024
Start date
15 Dec 2024
Primary completion date
1 Jul 2026
Lead sponsor
Ain Shams University
NCT number
NCT06728709

What you commit to

  • Study type: Observational
  • Participants enrolled: 280
  • From 15 Dec 2024 to the primary completion date, 1 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patient's refusal
  • inability to do a lung ultrasound examination during the first 24 hours of admission

Who the study is looking for

  • Any patient admitted to the obstetrics and gynecology intensive care unit

Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ain Shams University
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.