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Optimizing the Diagnosis of Acute Appendicitis

Optimizing the Diagnosis of Acute Appendicitis - Open, Randomized, Parallel Groups, Prospective Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04117061
Acronym
OPTIMA
Enrollment
200
Registered
2019-10-07
Start date
2018-12-01
Completion date
2021-05-01
Last updated
2019-10-07

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

Conditions

Acute Appendicitis

Brief summary

Aim of the study: to identify the signs of acute appendicitis delta signs - clinical, laboratory or ultrasound signs, whose change (delta) would allow to identify or deny the diagnosis of acute appendicitis without a computed tomography examination and thus to lower computed tomography rates.

Detailed description

This study consists of two parts: * In the first part investigators enroll all patients (except pregnant) that are refered to Vilnius University Hospital Santaros clinics with suspected acute appendicitis in order to get cohort data. All patient get primary clinical evaluation, laboratory tests (WBC, CRP) an ultrasound examination. * After primary evaluation if final diagnosis could not be made, and investigator still suspect acute appendicitis, participant is included in to randomised study part. * Randomised sudy part has two arms: control and observation groups. * Control group get the traditional diagnostic path - is refered to CT scan examination. * Observation group get repeated evaluation after 8-12 hours and only than is diagnosis stays unclear, patient gets a CT scan. * All patient are contacted after 30 days after visit to our hospital, to get information about their health status and possible additional visits to other hospitals or operations.

Interventions

PROCEDUREObservation

Patient after primary investigation is observed for 8-12 hours, (instead of being send directly to CT scan), after observation repeated clinical evaluation, laboratory tests and ultrasound examination are done , if final diagnosis stays unclear the patient is refered to CT scan.

Sponsors

Vilnius University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Open, randomized, parallel groups prospective study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient with the symptoms of acute appendicitis: pain in the right lower quadrant, pain migration from epigastrium to right lower quadrant, nausea, rebound pain, elevated temperature.

Exclusion criteria

for randomized part: * Pregnant patient. Inclusion Criteria for randomized part: * After primary clinical, laboratory and ultrasound examination diagnosis of acute appendicitis could not be confirmed or excluded. * No other gynecological, urological ir gastroenterological pathology is confirmed.

Design outcomes

Primary

MeasureTime frameDescription
Reduction of the CT scans number24 hourswhen performing alternative diagnostic protocol, that includes patient observation for short period we expect to reduce a number of CT scans performed, for the patients with suspected acute appendicitis.
Negative appendectomy rate30 daysWe expect the negative appendectomy rate will will not increase while using alternative diagnostic protocol that includes patient observation.

Secondary

MeasureTime frameDescription
Delta marker Alvarado acute appendicitis risk evaluation score12 hoursDelta marker Alvarado acute appendicitis risk evaluation score Tha changes in score over the time that might show higher or lower probability of possible acute appendicitis. Scale ranges decribe a prediction of having acute appendicitis: 1-4 33 % of having appendicitis, 5-6 66 % of hanving, 7-10 93 % of having appendicitis.
Delta marker White blood cell count12 hoursThe changes in white blood cell count over the time that might show higher or lower probability of possible acute appendicitis.
'Appendicitis Inflammatory Response (AIR) Score'12 hours'Appendicitis Inflammatory Response (AIR) Score') evaluates the risk for acute appendicitis. scale ranges are: 0-4 low probability outpatient follow up, 5-8 inermediate probability in hospital observation, 9-12 high probability, surgical treatment..
Delta marker changes in ultrasound results12 hoursThe changes in ultrasound findings over the time may progress and influence investigator to change opinion about the concusion. Repeated ultrasound diagnosis might change from unequivocal to acute apendicitis (and CT scan can be avoided then). We do use structured conclusions of the ultrasound exam, that might be: accute appendicitis; apendix visualised but changes are equivocal; apendix visualised uninflamed; apendix not visualised, but there are secondary findings; apendix not visualised and there is no secondary findings. We are going to measure the change in final ultrasound diagnosis over the time.
Delta marker CRP count12 hoursThe changes CRP level over the time that might show higher or lower probability of possible acute appendicitis.

Countries

Lithuania

Contacts

Primary ContactTomas Poskus, Professor.
tomas.poskus@santa.lt+37068678893
Backup ContactRaminta Luksaite, Phd student
raminta.luksaite@santa.lt+37068960611

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026