Using ultrasound to assess body composition in critically ill patients
Detection of the Changes in Body Composition of Critically Ill Obstetrics by Ultrasound and the Co-relations With Clinical Outcomes; a Prospective Observational Study.
This study is testing if ultrasound can help doctors see changes in body composition, like muscle loss and fluid shifts, in critically ill patients to improve their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 121 (estimated) |
| Ages | 16 Years and up |
| Sex | Female |
| Sponsor | Ain Shams University Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Cairo, Cairo Governorate) |
| Trial ID | NCT06728722 on ClinicalTrials.gov |
What this trial studies
This observational study aims to objectively assess changes in body composition among critically ill patients using ultrasound technology. The focus is on evaluating muscle loss and fluid shifts, which are critical factors affecting recovery in patients with acute illnesses, particularly in obstetrics and gynecology. By utilizing portable and radiation-free ultrasound, the study seeks to provide accurate measurements that can guide treatment strategies and improve clinical outcomes. The research highlights the importance of non-invasive techniques for monitoring muscle health and nutrition risk in intensive care settings.
Who should consider this trial
Good fit: Ideal candidates for this study are females aged 16 and older who are admitted to the obstetrics and gynecology critical care unit and classified as ASA class I, II, or III.
Not a fit: Patients who refuse to participate in the study will not benefit from the findings or interventions proposed.
Why it matters
Potential benefit: If successful, this study could lead to improved monitoring and management of muscle health and fluid status in critically ill patients, enhancing recovery outcomes.
How similar studies have performed: Previous studies have indicated that ultrasound measures of muscle loss can serve as effective biomarkers in critically ill patients, suggesting a promising approach for this research.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * females with age 16 with no upper limit * American Society of Anesthesiologists (ASA) class I, II or III, * admitted to the obstetrics and Gynecology critical care unit Exclusion Criteria: * Patient refusal
Where this trial is running
Cairo, Cairo Governorate
- Ain shams university — Cairo, Cairo Governorate, Egypt (Recruiting)
Study contacts
- Study coordinator: wessam selima, MD
- Email: w.z.selima@gmail.com
- Phone: 01001958858
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.