Allgemeine Informationen
  • Krankheitskategorie Blasenkrebs (BASEC)
  • Studienphase Phase 4 (ICTRP)
  • Rekrutierungsstatus Rekrutierung abgeschlossen (BASEC/ICTRP)
  • Studienstandort
    Bern
    (BASEC)
  • Studienverantwortliche Prof. Dr. med. Patrick Y. Wüthrich anaesthesie@insel.ch (BASEC)
  • Datenquelle(n) BASEC: Import vom 16.06.2025 ICTRP: Import vom 18.01.2024
  • Letzte Aktualisierung 16.06.2025 21:36
HumRes58992 | SNCTP000004932 | BASEC2022-00209 | NCT05391607

Influence of hyperoncotic 20% albumin, iso-oncotic 5% albumin, and Ringer's lactate on plasma volume expansion in hemorrhage during cystectomy. A prospective, randomized, controlled monocentric study. (VASCALB)

  • Krankheitskategorie Blasenkrebs (BASEC)
  • Studienphase Phase 4 (ICTRP)
  • Rekrutierungsstatus Rekrutierung abgeschlossen (BASEC/ICTRP)
  • Studienstandort
    Bern
    (BASEC)
  • Studienverantwortliche Prof. Dr. med. Patrick Y. Wüthrich anaesthesie@insel.ch (BASEC)
  • Datenquelle(n) BASEC: Import vom 16.06.2025 ICTRP: Import vom 18.01.2024
  • Letzte Aktualisierung 16.06.2025 21:36

Zusammenfassung der Studie

Bladder removal with urinary diversion is a major urological surgery during which blood loss may occur. To correct this, various infusion therapies are available. Often, so-called crystalloid infusion solutions, i.e., aqueous infusion solutions with dissolved salts, are used. However, these only remain in the bloodstream for a limited time before being either transferred to the tissue or excreted. Hyperoncotic solutions, such as 20% albumin, are also used. This means that it is an infusion solution in which, due to the increased proportion of dissolved protein, the binding or retention of free water in the bloodstream is increased. In healthy subjects, it has been shown that an infusion of this solution significantly increases blood plasma volume by mobilizing fluid from the tissue, and that this effect lasts for several hours. There is also an infusion solution, 5% albumin, which is referred to as iso-oncotic. This means that it is in equilibrium with the amount of protein also found in human plasma. We now want to investigate how strongly this effect can be demonstrated in the replacement of blood loss. We investigate how much blood volume increases when administering 3 ml/kg body weight of the 20% albumin solution or 12 ml/kg body weight of the 5% albumin solution and compare the results with a third group receiving crystalloid (saline) Ringer's lactate infusion solution.

(BASEC)

Untersuchte Intervention

With this study, we want to compare the influence of using an infusion solution for the replacement of blood loss during bladder removal on blood volume increase. The three infusion solutions are hyperoncotic albumin 20%, normo-oncotic albumin 5%, and the current so-called physiological solution, which has no oncotic effect. The aim of this study is to investigate and compare the effects of different fluid replacement therapies (hyperoncotic 20% albumin, iso-oncotic 5% albumin, and Ringer's lactate) during the hemorrhagic phase of the cystectomy procedure. The fluids will be administered using established fluid kinetics models, and their effect on volume and intravascular filling will be evaluated. We will assess hemodynamic parameters during the operation and evaluate other important biological parameters through blood samples. Complications occurring during the hospitalization period and within the first 30 days after surgery will also be analyzed.

(BASEC)

Untersuchte Krankheit(en)

Bladder cancer primarily occurs in older, polymorbid patients. The standard treatment for localized, muscle-invasive bladder cancer is cystectomy (bladder removal). Bladder removal with urinary diversion is a major urological surgery during which blood loss may occur. Intraoperatively, systemic inflammatory reactions are triggered by the procedure. The normal regulation of transcapillary fluid exchange is thereby disturbed. Additionally, hypovolemia is exacerbated by blood loss. Therefore, it is essential to replace this volume loss with the most efficient exogenous fluid supply.

(BASEC)

Kriterien zur Teilnahme
Individuals for whom bladder removal with urinary diversion is planned can participate. Additionally, they must be over 18 years old and provide their written consent. (BASEC)

Ausschlusskriterien
- Known hypersensitivity or allergy to the study drug - Significant renal insufficiency: GFR <60 ml/min/1.73 m² (Kidney Disease Outcomes Quality Initiative Stage 3 or higher) and use of diuretics. - Heart failure. (BASEC)

Studienstandort

Bern

(BASEC)

Switzerland (ICTRP)

Sponsor

nicht verfügbar

Kontakt für weitere Auskünfte zur Studie

Kontaktperson Schweiz

Prof. Dr. med. Patrick Y. Wüthrich

+41 31 632 21 11

anaesthesie@insel.ch

(BASEC)

Allgemeine Auskünfte

University Hospital Inselspital, Bern

(ICTRP)

Name der bewilligenden Ethikkommission (bei multizentrischen Studien nur die Leitkommission)

Ethikkommission Bern

(BASEC)

Datum der Bewilligung durch die Ethikkommission

11.05.2022

(BASEC)


ICTRP Studien-ID
NCT05391607 (ICTRP)

Offizieller Titel (Genehmigt von der Ethikkommission)
nicht verfügbar

Wissenschaftlicher Titel
Randomized Trial of Intraoperative Intravascular Effect of Hyper-oncotic 20% Albumin, Iso-oncotic 5% Albumin and Ringer Lactate During Haemorrhage in Cystectomy. A Prospective Randomized Active-controlled Single Centre Trial (ICTRP)

Öffentlicher Titel
Comparison Between Hyperoncotic and Isooncotic Albumin to Support Blood Loss Replacement (ICTRP)

Untersuchte Krankheit(en)
Blood Loss, Surgical
Fluid Retention
(ICTRP)

Untersuchte Intervention
Drug: Hyperoncotic Albumin 20%
Drug: Ringer's Lactate Crystalloid Solutions (control group)
Drug: Isooncotic Albumin 5%
(ICTRP)

Studientyp
Interventional (ICTRP)

Studiendesign
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label). (ICTRP)

Ein-/Ausschlusskriterien

Inclusion Criteria:

- Non emergent radical cystectomy with urinary diversion

- Adult: older than 18 years

- Written informed consent

Exclusion Criteria:

- Contraindications to the class of drugs under study (i.e: known hypersensitivity/
allergy to class of drugs or to the investigational product).

- Renal insufficiency: GFR: <60ml/min/1.73m2 (KDIGO Clinical Practice Guideline for
Acute Kidney Injury, stage 3 and over).

- History of heart failure.

- Use of diuretic treatment.

- Women who are pregnant or breast feeding (exclusion of surgery per se).

- Inability to follow the procedures of the study, e.g. due to language problems,
psychological disorders, dementia, etc. of the participant.

- Enrolment of the investigator, his/her family members, employees and other dependent
persons.
(ICTRP)

nicht verfügbar

Primäre und sekundäre Endpunkte
Plasma volume expansion
(ICTRP)

Endothelial damage
Biological markers (pro-ANP and pro-BNP)
Pleth variability index (PVI)
Cardiac output (CO)
Stroke volume (SV)
(ICTRP)

Registrierungsdatum
17.05.2022 (ICTRP)

Einschluss des ersten Teilnehmers
25.05.2022 (ICTRP)

Sekundäre Sponsoren
nicht verfügbar

Weitere Kontakte
Patrick Y Wuethrich, MD, University Hospital Inselspital, Bern (ICTRP)

Sekundäre IDs
VASCALB (ICTRP)

Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten
nicht verfügbar

Weitere Informationen zur Studie
https://trialsearch.who.int/Trial2.aspx?TrialID=NCT05391607 (ICTRP)

Ergebnisse der Studie

Zusammenfassung der Ergebnisse

nicht verfügbar

Link zu den Ergebnissen im Primärregister

nicht verfügbar