Diagnostic Importance of the C-reactive Protein From Blood and Saliva in Children With Acute Appendicitis
NCT ID: NCT06051825
Last Updated: 2023-09-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
100 participants
OBSERVATIONAL
2023-11-01
2024-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Salivary C- Reactive Protein, Mean Platelet Volume and Neutrophil Lymphocyte Ratio as Diagnostic Markers for Neonatal Sepsis
NCT04800445
New Protocol for Febrile Neonate Management
NCT03183531
Comparison of Salivary Procalcitonin (PCT) Levels and Serum PCT Levels
NCT06354205
Helicobacter Pylori Infection Among Women With Recurrent Abortion of Unknown Cause
NCT07293169
The Rate of C-reactive Protein (CRP) Increase as a Marker for Bacterial Infections in Children
NCT01159470
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients with acute appendicitis
Patients with acute appendicitis, after surgery and with pathohistological confirmation
Blood specimen collection for C-reactive protein (CRP) and WBC (white blood cells). Saliva specimen collection for analysis of CRP levels
Blood analysis of CRP and WBC levels Saliva analysis of CRP levels
Patients without acute appendicitis
Patients without acute appendicitis, after laboratory, clinical and/or radiological exclusion of acute admittance
Blood specimen collection for C-reactive protein (CRP) and WBC (white blood cells). Saliva specimen collection for analysis of CRP levels
Blood analysis of CRP and WBC levels Saliva analysis of CRP levels
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Blood specimen collection for C-reactive protein (CRP) and WBC (white blood cells). Saliva specimen collection for analysis of CRP levels
Blood analysis of CRP and WBC levels Saliva analysis of CRP levels
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* children with clinical signs of appendicitis
Exclusion Criteria
* children wich had previous abdominal surgery
* pregnancy
5 Years
17 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital of Split
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Klaudio Pjer Milunovic
principal investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Zenon Pogorelić, PhD.Prof
Role: PRINCIPAL_INVESTIGATOR
University Hospital of Split
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CHCSplit
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.