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Low-dose Contrast Media for Low-kVp Abdomen CT

Optimizing Low-dose Contrast Media Protocol for Low-kVp Abdominopelvic CT in Suspected Acute Appendicitis

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05878665
Enrollment
109
Registered
2023-05-26
Start date
2023-12-21
Completion date
2026-09-04
Last updated
2026-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Appendicitis Acute

Keywords

acute appendicitis, acute abdomen, CT

Brief summary

The purpose of this clinical study is to test the performance of low radiation dose abdominal CT combined with low dose contrast media for the diagnosis of acute appendicitis in young patients. The main questions to be answered are: 1. Can low-dose contrast media paired with low-dose radiation CT of the abdomen provide acceptable diagnostic accuracy in acute appendicitis? 2. How much radiation dose can be saved by using low radiation dose abdominal CT in combination with low dose contrast media?

Interventions

DIAGNOSTIC_TESTWeight-adjusted low-dose contrast media paired with low-radiation dose abdomen CT

The investigators are aiming for a 10% reduction in iodine dosage at 10 kVp reduction in CT radiation. Routine iodine dosing is 0.521 g I/kg at 120 kVp. Therefore, at 90 kVp, a 30% reduction in iodine dosing is expected, which is 0.365 g I/kg. At 100 kVp, the iodine dosage is reduced to 0.417 g I/kg, which is a 20% reduction. The kVp value is automatically selected by the CT device according to the body habitus, which is a clinical routine.

Sponsors

Bohyun Kim
Lead SponsorOTHER
GE Healthcare
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to 44 Years
Healthy volunteers
No

Inclusion criteria

* Patients in the emergency department with suspected acute appendicitis based on clinical examination * Patients scheduled for contrast-enhanced CT of the abdomen and pelvis for diagnosis of suspected acute appendicitis.

Exclusion criteria

* Patients who decline to participate * Contraindications to contrast-enhanced CT (eGFR \< 30 mL/min/173 m\^2 or pregnant) * BMI \>= 30.

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic accuracy for acute appendicitisFor operated patients, postop. period (up to 1 month); If non-operated, at 6 months-FUThe primary outcome of the study is the diagnostic accuracy of double low-dose CT for acute appendicitis in young adults with suspected acute appendicitis. Based on the CT findings, a three-tiered diagnosis of appendicitis will be given (no appendicitis, uncomplicated appendicitis, or complicated appendicitis). In the case of no appendicitis, a possible alternative diagnosis is given. The reference standard for appendicitis is operative findings and surgical pathology reports. In nonoperative cases, sequential radiologic evaluation, clinical follow-up, and the judgment of the attending physician will conclude the diagnosis. Specifically, if the patient is not treated for recurrent symptoms within 6 months, the radiologic diagnosis of CT findings is considered valid. The diagnostic accuracy for acute appendicitis is true positive for acute appendicitis and true negative for acute appendicitis divided by all participants.

Countries

South Korea

Contacts

PRINCIPAL_INVESTIGATORBohyun Kim, MD, PhD

Seoul St. Mary's Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 10, 2026