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Clinical Trials in Denmark / NCT05679557
Recruiting Not applicable

Comprehensive Geriatric Assessment for Perioperative Optimization in Cystectomy

NCT05679557 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2023-02-01
Last updated
2026-02-27

Condition(s) studied

Bladder Cancer

Investigational drug(s) / intervention(s)

Perioperative geriatric assessment and intervention

Perioperative geriatric assessment and intervention: The intervention will comprise a preoperative, thorough geriatric, multidisciplinary assessment (CGA) and tailored interventions, focused on optimizing health issues of expected importance in further course of surgery. Furthermore, postoperative ward rounds by a geriatric team will be conducted. Thus, the course of treatment for each patient will be a close interdisciplinary collaboration.

Study summary

Patients with muscle-invasive bladder cancer are often older and multimorbid, thus in an increased risk of perioperative mortality and morbidity in relation to radical cystectomy (RC). The aim of the study is to investigate the effect of perioperative Comprehensive Geriatric Assessment (CGA) and tailored intervention in older, frail patients with bladder cancer undergoing RC.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Patients with muscle-invasive bladder cancer and scheduled radical cystectomy. 2. Planned urinary diversion with an ileal conduit 3. Age ≥ 65 years. 4. Patients considered frail by G8 screening tool (total score ≤14). Exclusion Criteria: 1. Patients who refuse or are not able to provide informed consent. 2. Patients who do not speak or understand Danish. 3. Planned concomitant nephroureterectomy or other major surgical intervention at the same time as RC

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Odense University Hospital Odense Denmark Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05679557 on ClinicalTrials.gov ↗ ← All trials in Denmark