NCT07196553

Brief Summary

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

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
125

participants targeted

Target at P50-P75 for all trials

Timeline
16mo left

Started Oct 2025

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress32%
Oct 2025Oct 2027

First Submitted

Initial submission to the registry

September 13, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

September 29, 2025

Completed
2 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2027

Last Updated

September 29, 2025

Status Verified

September 1, 2025

Enrollment Period

1.9 years

First QC Date

September 13, 2025

Last Update Submit

September 20, 2025

Conditions

Ultrasound in Ascites

Outcome Measures

Primary Outcomes (1)

  • Role of ultrasound in ascites

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

    Baseline

Other Outcomes (1)

  • role of ultrasound in ascites

    Baseline

Interventions

UltrasoundDEVICE

ultrasound examination

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

-Patients attending Assiut University Hospital from different age groups and both sexex with clinically suspected ascites referred for abdominal ultrasound.

You may qualify if:

  • 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.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Ultrasonography

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Study Officials

  • Sami Abdel-Aziz Khalil, proffesor

    Assiut University

    STUDY DIRECTOR

Central Study Contacts

Esraa Mohamed Abdelaziz

CONTACT

+201015039486es2011es99@gmail.com

Hayam Yahia Khalil, lecturer

CONTACT

+201067949776Hayamyahia1989@gmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
15 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

September 13, 2025

First Posted

September 29, 2025

Study Start

October 1, 2025

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

October 1, 2027

Last Updated

September 29, 2025

Record last verified: 2025-09