Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07196553

Ultrasound and Ascites

The aim of this study is to evaluate the role of ultrasound in the detection, characterization, and determination of the underlying cause of ascites in patients attending Assiut University Hospital

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Sex eligibility

All sexes

Study type

Observational

About this study

Normally, the peritoneal cavity contains 25-50 mL of ascitic fluid, which allows for the movement of bowel loops past one other and helps hydrate serosal surfaces. Ascites is defined as the pathological accumulation of excess fluid in the peritoneal cavity.

More than one cause may be responsible for the development of ascites (multifactorial), liver cirrhosis remains the leading cause (≈85% of cases), followed by many causes such as malignant neoplasia, tuberculous infection, cardiac insufficiency, renal diseases ,trauma and other infectious, inflammatory and hemorrhagic causes ,multiple etiologies may coexist.

once ascites develops, it carries a risk of further serious complications such as acute spontaneous bacterial peritonitis (SBP) (Occurs in 10-30% of hospitalized cirrhotic patients with ascites and associated with high morbidity and mortality rate), hepatorenal syndrome, hepatic hydrothorax, respiratory compromise and other compliactions including gastrointestinal, circulatory , metabolic complications….etc Medical history, physical examination, abdominal ultrasound, blood tests, and a diagnostic paracentesis for ascitic fluid analysis should all be part of the initial assessment of ascites. Ascites can be detected on physical examination using traditional shifting dullness to percussion when there is approximately 500 ml of fluid. However, in an increasingly obese population, there is limited reliability on clinical examination findings alone.

Trans-abdominal US (TAUS) can easily demonstrate large volumes of fluid and, with a meticulous technique, much smaller volumes can also be detected making an excellent first-line imaging tool, safe, inexpensive, and widely available, It's also superior to CT in qualitative assessment-distinguishing between simple (anechoic) and complex (particulate or septated) ascites.Portable ultrasound devices further enable reliable, bedside diagnosis.

Ultrasound is also used in ultrasound-guided aspiration and paracentesis which is essential for safely obtaining ascitic fluid for determining the underlying etiology (via Serum-Ascites Albumin Gradient (SAAG), cytology, biochemical analysis) and detecting complications such as spontaneous bacterial peritonitis,The presence of septations or debris in ascites fluid can be suggestive of infected ascites.

The most important diagnostic study of any patient being evaluated for SBP or being admitted to the hospital with ascites and cirrhosis is a paracentesis. In a US national inpatient study of over 31,000 patients admitted with cirrhosis and ascites where about one-half underwent a paracentesis, the mortality rate for patients who underwent a paracentesis was significantly lower than for those who did not have one (6.3% vs 8.9%). hemorrhagic ascites, or malignant recurrence.

Real-time ultrasound improves diagnostic accuracy and reduces complication rates compared with landmark-based aspiration..Using ultrasound guidance for paracentesis significantly reduces complication rates, such as bleeding and infection.complication rates drop from ~4.7% (landmark-based) to ~1.4% with ultrasound.

therapeutic paracentesis is established as the first-line treatment for patients with large or refractory ascites providing rapid symptom relief and improving quality of life. It is safe when done under ultrasound guidance with albumin replacement for large-volume drainage.

' We chose to carry out this study to evaluate the specificity, sensitivity, accuracy, and positive and negative predictive value of role of ultrasound in detection of ascites and evaluation of the underlying cause.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient from different age groups and both sexex will be included in our study.
  • Patients with clinically suspected ascites referred for abdominal ultrasound.
  • Patients who will provide informed consent for participation.

Exclusion criteria

  • Patients with a history of recent abdominal surgery (<1 month).
  • Patients with inadequate ultrasound visualization due to severe obesity or extensive bowel gas.
  • Patients who will decline to participate

Treatment and study plan

Ultrasound

Device

ultrasound examination

Primary outcomes

  1. Role of ultrasound in ascites

    Time frame: Baseline

    To evaluate the accuracy of ultrasound in ascites detection and characterization.

Other outcomes

  1. role of ultrasound in ascites

    Time frame: Baseline

    to evaluate the role of ultrasound in the detection, characterization, and determination of the underlying cause of ascites in patients attending Assiut University Hospital

Study contacts

Contact information is provided by the study sponsor or research team.

Esraa Mohamed Abdelaziz

CONTACT

[email protected]

+201015039486

Hayam Yahia Khalil, lecturer

CONTACT

[email protected]

+201067949776

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Role of Ultrasound in Ascites: Detection, Characterization, and Evaluation of the Underlying Cause.

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Sep 29, 2025
Registry last updated
Sep 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.