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NCT Number: NCT07008261

Robot-assisted Cystectomies With Regard to Blood Loss, Pain and Transfusions.

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • planned radical cystectomy

Exclusion criteria

  • ASA classification V
  • Previously known coagulation disorder

Treatment and study plan

Primary outcomes

  1. perioperative blood loss

    Time frame: 6 hours

    perioperative blood loss

Secondary outcomes

  1. Preoperative iron deficiency

    Time frame: up to 4 weeks prior surgery

    Preoperative messured iron deficiency

  2. RBC transfusion

    Time frame: perioperative up to hospital discharge or death (up to 4 weeks)

    Number of RBC transfusions

Study contacts

Contact information is provided by the study sponsor or research team.

Armin Flinspach N PD. Dr. med. habil., M.D.

CONTACT

[email protected]

+49 69 6301 84136

Sponsors and collaborators

Lead sponsor

Goethe University

Other

Registry information

Official study title

Prospective Evaluation of Robot-assisted Cystectomies With Regard to Blood Loss, Pain and Transfusion Requirements.

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jun 6, 2025
Registry last updated
Sep 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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