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Diagnostic Algorithm for Appendizitis (DIALAPP)

Evaluation of Diagnostic Algorithm for Suspected Acute Appendicitis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02627781
Acronym
DIALAPP
Enrollment
400
Registered
2015-12-11
Start date
2015-11-30
Completion date
2018-05-31
Last updated
2016-09-01

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

Conditions

Reduction of Negative Appendectomy Rate

Keywords

acute appendicitis, Alvarado Score, negative appendectomy, right abdominal pain

Brief summary

The diagnosis of acute appendicitis remains a challenge in daily clinical practice. The high incidence of appendicitis drives the need to reduce morbidity and unnecessary costs due to negative appendectomies. The aim of the present observation study is to evaluate a diagnostic and therapeutic algorithm for suspected acute appendicitis. The investigators believe that this diagnostic algorithm helps to simultaneously avoid unnecessary operations, costs and radiation exposure.

Detailed description

This prospective observation study will be performed in the university hospital Frankfurt with a 24-h emergency service, with surgery and radiology readily available. The data will be compiled on patients older than 18 years who will be admitted to the emergency unit with suspected appendicitis. During the study period, the clinical workflow is standardized. In all cases a resident of surgery and/or consultant surgeon clinically evaluate and perform an ultrasound scan on all patients with suspected appendicitis. With the use of clinical and laboratory results the physician (surgeon) will calculate the Alvarado Score and depending on the result the next diagnostic steps or the treatment will be chosen. Additionally, the department of gynecology of the university hospital routinely evaluate all women of childbearing age. Upon other terms following variables will be collected: age, gender, white blood cells (WBC), C-reactive protein (CRP), Alvarado Score, visuell pain scale, CT scan results, pathologic findings, time between admission and operation, operation procedure, treatment and diagnosis of patients without operation, length of hospital stay, and 30-day complication rate. Furthermore, there will be a follow-up of all patients (with and without operation) after 30 days and 6 months. The investigators assume that the use of a diagnostic and therapeutic algorithm reduces unnecessary negative appendectomies and optimizes the duration of the hospital stay and the costs.

Interventions

None listed

Sponsors

Goethe University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* complete evaluation, examination and diagnostic pathways of the patients with suspected appendicitis in our University Hospital

Exclusion criteria

* appendectomy during other operations

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of the negative appendectomy rate6 monthsIn this part of the study, the negative appendectomy rate will be determined. A negative appendectomy is characterized by normal findings in the pathological examination and therefore constitutes a medically unnecessary appendectomy.

Secondary

MeasureTime frameDescription
The influence of computed tomography for the diagnosis of acute appendicitis30 daysIn this part of the study the investigators evaluate the careful and cost-effective integration of computed tomography in the clinical pathway.
Incidence of readmission to hospital6 monthsIn this part of the study the readmission rate to hospital will be evaluated because of postoperative complications, infections and continuous abdominal pain will be included.
Evaluation of postoperative complications6 monthsIn all patients, who received an appendectomy the postoperative complication rate will be recorded. In statistical analysis factors, which are associated with complications will be analyzed.

Countries

Germany

Contacts

Primary ContactJuliane Liese, MD
juliane.liese@kgu.de+496963015251
Backup ContactAlexander Reinisch, MD
alexander.reinisch@kgu.de+4963016502

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026