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CompletedNCT04572204Updated Feb 8, 2023

Management of Grades 3-5 Renal Trauma in Pediatrics

An observational study in Renal Trauma, sponsored by Assiut University. Completed at 1 site in Egypt. Open to participants aged 0 Years to 18 Years. Per ClinicalTrials.gov, last updated 2023-02-08.

Sponsored by Assiut University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
33
Ages
0 Years to 18 Years
Sex
All
01

Study summary

comparing conservative management versus interventional management in hemodynamically stable paediatric patient with blunt renal trauma, evidence suggests that there is a reduced rate of renal loss and blood transfusion in patients managed conservatively.

02

Conditions studied

  • Renal Trauma

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03

In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's enrollment of 33 is below the median of 135 across 1,597 observational studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.

Of its 13 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
0 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

60 children (age group 0-18 years) will be added to my study divided into two groups regardless of sex

Inclusion criteria

  • Children ( age group 0-18) who are diagnosed to have renal tissue injury grade 3-5 by contrast CT

Exclusion criteria

Exclusion Criteria:

  • Age group more than 18 years
  • Low grade renal trauma 1-2
  • Patients who get explored due to extra urologic indication without proper urologic assessment
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
33 participants (actual)
Patient registry
No

Groups and cohorts

  • Conservative group
  • interventional group

    Other: Surgical

Interventions

  • OtherSurgical

    Minimal: Such as PCN insertion Endosopic: Such as DJ insertion Surgical: Repair, Partial or total nephrectomy Angioembolization

06

What researchers measure

Primary outcomes

  1. Stabilization of haemodynamic status of the patient in the first 24-72 hours

    Time frame: 24 to 72 hours

Secondary outcomes

  1. Resolution of perinephric collection during follow up Triphasic MSCT abdomen and pelvis

    Time frame: 1 year

07

Study locations

1 site
  • Assiut University
    Assiut, 71717, Egypt
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 8, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04572204
Lead sponsor
Assiut University
Responsible party
Ahmed Hamdan Gameel (Resident doctor, Assiut University) — Principal investigator
First posted
Oct 1, 2020
Start date
Oct 1, 2020
Primary completion
Sep 30, 2022
Completion
Oct 30, 2022
Last update
Feb 8, 2023

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 completed, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

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