Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:30 AM
Ignite Modification Date:
2025-12-25 @ 2:30 AM
NCT ID:
NCT05392634
Eligibility Criteria:
Inclusion Criteria:
* histologically confirmed diagnosis of very high risk non muscle-invasive bladder carcinoma (cT1NoMo) or muscle-invasive bladder carcinoma (cT2-T4NxM0) with or without neoadjuvant therapy (chemotherapy or immunotherapy are both possible);
* patient should be eligible for radical cystectomy (RC) + pelvic lymph node dissection (PLND), and agreement to undergo curative intent standard RC + PLND (including prostatectomy or hysterectomy if applicable) according to surgeon opinion;
* pelvic lymph node dissection is engaged in two possible variants: extended level to intersection of ureter and iliac vessels; superextended level - up to aortic bifurcation;
* urinary diversion is engaged in two possible variants: orthotopic diversion (J- or U-pouch reservoirs), heterotopic diversion in the Mainz-I modification, Bricker;
* male or female is at least 18 years old at the time of signing the informed consent form;
* female patient is eligible to participate if she is not pregnant, not breastfeeding;
* ECOG performance status of 0 or 1;
* adequate organ function (in accordance with laboratory standards);
* used valid protocol for Enhanced Recovery After Surgery (ERAS protocol) at Hospital (oncourological department);
Exclusion Criteria:
* known additional non-urothelial malignancy that is progressing or has required active anticancer treatment ≤3 years of study randomization, with certain exceptions;
* diagnosis of immunodeficiency or receipt of chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior the first dose of study drug;
* replacement doses of corticosteroids are permitted for participants with adrenal insufficiency;
* evidences of uncontrolled diseases (diabetes mellites, noninfectious pneumonitis that required steroids, et.) or any conditions which interfere with the conduct of the research procedures according to doctor opinion;
* presence of 2 or more criteria for systemic inflammatory response syndrome (SIRS) at the time of the patient's admission to the hospital (assessment of these factors 3-7 days before randomization):
* temperature ≥ 38˚С or ≤ 36˚С;
* heart rate (HR) ≥ 90 / min;
* respiratory rate \< 20/min or hyperventilation (Pa CO2 ≤ 32 mm Hg);
* blood leukocytes \>12 ∙ 109 / l or \< 4 ∙ 109 / l, or immature forms \> 10%
* prohibited urinary diversion when planning surgery and signing voluntary consent: diversion into continuous intestine (ureterosigmostomy, Mainz-pouch II operation);
* inadequate organ function:
* Neutrophils \<1.5 x 10 \^ 9 / l
* Platelets \<100 x 10 \^ 9 / l
* ALT\> 3 x VGN
* AST\> 3 x VGN
* Bilirubin\> 1.5 x ULN
* GFR level \<35 ml / min
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
90 Years
Study:
NCT05392634
Study Brief:
Protocol Section:
NCT05392634