Robot-assisted Cystectomies With Regard to Blood Loss, Pain and Transfusions.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Transfusions, Cystectomy, Blood Loss Requiring Transfusion, Anaemia. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Prospective Evaluation of Robot-assisted Cystectomies With Regard to Blood Loss, Pain and Transfusion Requirements.
Overview
What influence does robot-assisted surgical treatment in the sense of a radical cystectomy and possibly bladder reconstruction have on blood loss, pain and transfusion requirements? We intend to conduct a corresponding prospective observational study at a tertiary centre.
Primary outcome measures
- perioperative blood loss [Time frame: 6 hours]
Secondary outcome measures (2)
- Preoperative iron deficiency [Time frame: up to 4 weeks prior surgery]
- RBC transfusion [Time frame: perioperative up to hospital discharge or death (up to 4 weeks)]
Eligibility criteria
Inclusion criteria
- planned radical cystectomy
Exclusion criteria
- ASA classification V
- Previously known coagulation disorder
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Germany · 1 center
- Uniklinikum — Frankfurt am Main
Identifiers
NCT: NCT07008261 · PBM in robot cystectomies