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NCT05931458Not yet recruiting

AppenDectomy Vs ANti TNF-a in Inducing Clinical and EnDoscopic Remission in Left-sided Ulcerative Colitis

ADVANCED-UC TRIAL: AppenDectomy Vs ANti TNF-a in Inducing Clinical and EnDoscopic Remission in Left-sided Ulcerative Colitis - A Randomized Clinical Trial

Source: ClinicalTrials.gov · Last updated 5 Jul 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Ulcerative Colitis (UC) is a chronic Inflammatory Bowel Disease (IBD) characterized by a multifactorial etiology, a variable involvement of large bowel, and a relapsing-remitting course. In order to keep the disease in a "quiescent" status and to prevent relapses, a significative percentage of UC patients will remain on long-term drug therapy. However, long-term immunosuppressant therapy is not free of risks and complications: in fact, these therapies have an impact on both healthcare system resources and patients' quality of life; more, there are even concerns regarding the side effects of long-term immunosuppressant therapy. Over the past 20 years, a considerable amount of evidence was produced to support the immunomodulatory role of the appendix in the development and course of UC: there is a strong inverse relationship between previous appendectomy and development of the UC. One of the proposed theories to justify this link is that the appendix could act as a reservoir for commensal bacteria that can be secreted into the colon, affecting its microbiome and immunological response; another theory describes the appendix as the "priming site" for the cytokine production and the immunological cascade that may trigger inflammation in colon and rectum. The idea of this study moves from these assumptions: the investigators aim to evaluate the impact of appendectomy in patients with UC who are candidates to the treatment with biologics (Anti TNF-a), because of conventional therapies failure. To further reduce any ethical problems and significantly lower any surgical morbidity, investigators will restrict the study population to only patients with active left-sided colitis, so that the surgery for appendectomy will take place on a non-inflamed cecum. By undertaking this study, the investigators hope to a) learn more about the role of appendix and the impact of appendectomy in the clinical history of Ulcerative Colitis; b) demonstrate that laparoscopic appendectomy, a relatively simple surgical procedure that can also be performed in day-surgery with a very low expected complication rate, is a treatment that is superior to biological therapy, avoiding patients starting a chronic, long-lasting therapy, with the consequent risk of immunosuppression, and with possible higher costs for the health system in the long term.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
94 (estimated)
First submitted
18 Jun 2023
Start date
1 Jul 2023
Primary completion date
1 Jul 2024
Lead sponsor
Federico II University
NCT number
NCT05931458

What you commit to

  • Study type: Interventional
  • Planned participants: 94
  • From 1 Jul 2023 to the primary completion date, 1 Jul 2024
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who previously received appendectomy
  • Patients who have had previous laparotomic abdominal surgery, which could make the appendectomy more complex
  • Patients who receive a different surgical procedure from appendectomy because of intraoperative complications

Other illness

  • Lack of diagnostic certainty of Ulcerative Colitis / Crohn's disease diagnostic doubt

Age

  • Patients under the age of 18

Other

  • Patients with Severe Acute Colitis/Toxic Megacolon
  • Patients who have not given their consent to the intervention
  • Pregnant patients

Who the study is looking for

  • Patients aged 18 or above
  • Patients with a confirmed diagnosis of left-sided UC (extended up to the mid transverse colon)
  • Patients with active disease refractory to conventional treatment and candidates for anti- TNF-a treatment
  • Patients who have given consent to the surgical procedure

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.