ClinicalTrials.gg
Status unknownNCT03259048Updated Aug 23, 2017

Role of Ultrasound in Diagnosis of Acute Abdomen in Pediatric Group

An observational study in Ultra Sound in Diagnosis of Acute Abdomen in Pediatric Group, sponsored by Assiut University. Status unknown. Open to participants aged 1 Day to 18 Years. Per ClinicalTrials.gov, last updated 2017-08-23.

Sponsored by Assiut University · Observational

The sponsor has not verified this record recently (last verified Aug 2017), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
1 Day to 18 Years
Sex
All
01

Study summary

Acute abdomen can be defined as "A syndrome induced by wide variety of pathological conditions that require emergent medical or more often surgical management" [1].There are a plethora of causes that can lead to acute abdomen in children, they vary depending on the ages of the children and can be divided into diseases that can be treated with medical care and those in which emergency surgical intervention must be considered [2]. Ultrasonography is the initial choice in the diagnosis of the different causes of acute abdomen in children [3, 4]. It is very useful as it is non-invasive, cost- effective, repetitive, with no radiation exposure, as good as laparoscopy, can be done even in patients with scarred abdomen [5].

Read the detailed description

-Patient preparation:

  • No specific preparation is needed.
  • Demographic data including age, sex, detailed history, clinical presentation, laboratory tests, and data of any other investigations or operation will be obtained.
  • Clinical examination will be done in emergency pediatric unit for provisional diagnosis.

    -Study instruments:• Patients will examined by Grey-Scale Ultrasonography (U/S) combined with Color Doppler Ultrasonography (CDUS).

    3-Technique of examination

  • will be in supine position.
  • Patient First examination of whole abdomen will be done by Grey -Scale U/S using both 3.5 MHZ and 7.5 MHZ transducers .It will be done in both longitudinal ( parallel to long axis of the patient ) and transverse ( perpendicular to long axis of the patient ) orientation .
  • Then finally examination by Color Doppler US will be done for assessment of organ perfusion and diagnosing inflammation.
02

Conditions studied

  • Ultra Sound in Diagnosis of Acute Abdomen in Pediatric Group

Browse trials for

03

In context

Abdomen, Acute

65 studies on the registry are indexed under Abdomen, Acute; 14 are open to participants now.

This study's planned enrollment of 100 is below the median of 233 across 36 observational studies indexed under Abdomen, Acute.

Browse Abdomen, Acute studies →

Lead sponsor

Assiut University is the lead sponsor of 5,079 studies on the registry; 2,177 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients referred from the emergency Pediatric Unit for the assessment of the cause of acute abdomen from age of 1 day to 18 years.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • -In this study, 100 patients referred from the emergency Pediatric Unit for the assessment of the cause of acute abdomen.

Exclusion criteria

Exclusion Criteria:

    • Patients of age group above 18 years
  • Patients with trauma.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • pediatric group

    pediatric group from age of one day to eighteen years.

    Diagnostic Test: Abdominal ultrasound

Interventions

  • Diagnostic testAbdominal ultrasound

    Abdominal ultrasound will be used in the diagnosis of acute abdomen in pediatric group.

06

What researchers measure

Primary outcomes

  1. efficacy of ultrasound in diagnosis of acute abdomen

    efficacy of ultrasound in diagnosis of acute abdomen

    Time frame: 2 years

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2017; primary completion for Oct 2019, 24 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 19, 2017
First posted
Aug 23, 2017
StartEst.
Oct 1, 2017
Primary completionEst.
Oct 1, 2019
CompletionEst.
Oct 1, 2019
Last update
Aug 23, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 23, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03259048
Lead sponsor
Assiut University
Responsible party
mohmed abdelwahab (Resident of Radiology Department - Assiut University, Assiut University) — Principal investigator
First posted
Aug 23, 2017
Start date
Oct 1, 2017 (estimated)
Primary completion
Oct 1, 2019 (estimated)
Completion
Oct 1, 2019 (estimated)
Last update
Aug 23, 2017

Study contacts

mohamed abdelwahab
Contact
mohmed_abdelwahab1011@yahoo.com
01016307405
mohamed abdelwahab
Contact
mohmed_abdelwaab1011@yahoo.com
01016307405

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion