Inflammatory biomarkers in blood and appendix tissue in acute appendicitis
Official title: Evaluation of Systemic and Tissue Level Inflammatory Response in Acute Appendicitis Using Multiple Biomarkers
Run by Haydarpasa Numune Training and Research Hospital · NCT07926165 · Data updated 2026-11-12
This study tests whether blood and appendix tissue biomarkers correlate with how severe a patient’s acute appendicitis is, to help distinguish uncomplicated from complicated cases.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Haydarpasa Numune Training and Research Hospital Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Istanbul, Istanbul) |
| Status | Recruiting |
| Started | July 12, 2026 |
| Main results expected | January 12, 2027 |
| Study ends | May 27, 2027 |
| Registry record updated | November 9, 2026 |
| Trial ID | NCT07926165 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–65 with suspected acute appendicitis who are scheduled for appendectomy and can consent, with suitable tissue and clinical data available.
✕Probably not a fit
Patients without a favorable biomarker profile or those not experiencing varied inflammatory responses may not see a direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective observational study recruits adults with suspected acute appendicitis who are scheduled for appendectomy. It measures multiple inflammatory biomarkers in blood and in appendix tissue, and analyzes their relationships with disease severity and standard clinical findings. The goal is to see if tissue and systemic biomarkers together reflect the level of inflammation and can improve severity assessment beyond current methods. The intervention is limited to the surgical procedure (appendectomy) and biomarker analyses on collected specimens. Enrollment is at an Istanbul hospital with defined inclusion and exclusion criteria to ensure reliable data.
Why it matters
Potential benefit: If successful, findings could improve preoperative assessment and decision-making for acute appendicitis by better predicting which patients have uncomplicated versus complicated disease.
How similar studies have gone: Previous work has explored systemic markers like CRP and NLR in appendicitis, but this study adds tissue biomarkers to better reflect local inflammation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Adults aged 18-65 years. Willingness to participate in the study and provision of written informed consent. Suspected acute appendicitis based on clinical, laboratory, and/or imaging findings. Scheduled for appendectomy following general surgical evaluation. Availability of an appendectomy specimen suitable for postoperative histopathological examination. Availability of sufficient clinical and laboratory records for study evaluation. Exclusion Criteria: Age younger than 18 years or older than 65 years. Refusal to participate or failure to provide written informed consent. Presence of an active infection that may affect the systemic inflammatory response during the preoperative period. Concomitant active infectious diseases, including pneumonia, urinary tract infection, or sepsis. Chronic inflammatory or autoimmune diseases, including rheumatoid arthritis, inflammatory bowel disease, or systemic lupus erythematosus. History of malignancy or active malignancy. Chronic renal failure or advanced liver failure. Use of immunosuppressive therapy. Use of corticosteroids, chemotherapy, or biological agents. Preoperative use of antibiotics or anti-inflammatory medications at a level that may significantly affect inflammatory biomarker measurements. Pregnancy or breastfeeding. Identification of additional intra-abdominal pathology unrelated to appendicitis during appendectomy. Failure to confirm acute appendicitis on postoperative histopathological examination. Inadequate biological sample quantity or failure to store biological samples under appropriate conditions.
Where it's running
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Haydarpaşa Numune Training and Research Hospital
Istanbul, Istanbul, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Emre B Akçay
- Email: dr.eberatakcay@gmail.com
- Phone: +90 535 711 92 21
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.