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Robotic Radical Cystectomy Outcomes

19. mai 2021 oppdatert av: Simone Morselli, University of Florence

Impact of Robotic Surgery on Post-operative Outcomes of Patients Who Underwent Radical Cystectomy

Currently, in the treatment of bladder cancer the use of robotics has entered in clinical practice, therefor robotic radical cystectomy with or without reconstruction is offered to patients during counseling procedures, if deemed appropriate and possible. The aim of the study is therefore the long-term evaluation of the peri-post-operative, oncological and functional results of patients undergoing radical cystectomy, both with an open and robotic approach. This study will thus help to clarify the actual impact of robotic surgery

Studieoversikt

Studietype

Observasjonsmessig

Registrering (Forventet)

500

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

    • Tuscany
      • Florence, Tuscany, Italia, 50134
        • Rekruttering
        • Careggi University Hospital
        • Underetterforsker:
          • Mauro Gacci, MD
        • Underetterforsker:
          • Riccardo Campi, MD
        • Ta kontakt med:
        • Hovedetterforsker:
          • Simone Morselli, MD
        • Underetterforsker:
          • Maria Rosaria Raspollini, MD
        • Hovedetterforsker:
          • Arcangelo Sebastianelli, MD
        • Underetterforsker:
          • Donata Villari, MD
        • Underetterforsker:
          • Graziano Vignolini, MD
        • Underetterforsker:
          • Saverio Giancane, MD
        • Underetterforsker:
          • Pietro Spatafora, MD

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

The study population is made up of patients who underwent radical cystectomy at AOU Careggi, SOD Robotic Urological Surgery, Minimally Invasive and Renal Transplantation.

Beskrivelse

Inclusion Criteria:

  • Age major or equal 18 years
  • Patients who will undergo radical cystectomy
  • Consent to participate

Exclusion Criteria:

  • Absence of willingness to participate
  • Further refusal to participate to the study

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Radical Cystectomy
Patients who underwent radical cystectomy for bladder cancer in our centre
All the patients enrolled have undergone or will undergo radical cystectomy, with or without lymphadenectomy or urethrectomy All possibles urinary diversion are included, like ileal conduit, neobladder etc...

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of participants who will die from bladder cancer
Tidsramme: From enrollment to late follow-up, up to 7 years
Bladder Cancer Specific Mortality after surgery
From enrollment to late follow-up, up to 7 years
Number of participants who will experience bladder cancer recurrence
Tidsramme: From enrollment to late follow-up, up to 7 years
Bladder Cancer Recurrence
From enrollment to late follow-up, up to 7 years
Number of participants who will die from all causes
Tidsramme: From enrollment to late follow-up, up to 7 years
All cause mortality after surgery
From enrollment to late follow-up, up to 7 years

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of participants who will die from bladder cancer after Robotic Surgery
Tidsramme: From enrollment to late follow-up, up to 7 years
Robotic surgery specific impact on survival
From enrollment to late follow-up, up to 7 years
Number of participants who will experience bladder cancer recurrence after Robotic Surgery
Tidsramme: From enrollment to late follow-up, up to 7 years
Robotic surgery specific impact on recurrence
From enrollment to late follow-up, up to 7 years
Number of participants who will experience surgical complications after Robotic Surgery
Tidsramme: From enrollment to late follow-up, up to 7 years
Robotic surgery specific impact on surgical complications
From enrollment to late follow-up, up to 7 years
Variation in Quality of Life questionnaire after Robotic Surgery
Tidsramme: From enrollment to late follow-up, up to 7 years
Robotic surgery specific impact on quality of life according to European Organisation for Research and Treatment of Cancer (EORTC) core quality of life questionnaire (QLQ-C30)
From enrollment to late follow-up, up to 7 years
Variation in Quality of Life questionnaire according to Urinary diversions
Tidsramme: From enrollment to late follow-up, up to 7 years
Urinary diversion specific impact on quality of life according to European Organisation for Research and Treatment of Cancer (EORTC) core quality of life questionnaire (QLQ-C30)
From enrollment to late follow-up, up to 7 years
Number of participants who will experience surgical complications according to Urinary diversions
Tidsramme: From enrollment to late follow-up, up to 7 years
Urinary diversion specific impact on surgical complications
From enrollment to late follow-up, up to 7 years
Number of participants who will experience bladder cancer recurrence according to Urinary diversions
Tidsramme: From enrollment to late follow-up, up to 7 years
Urinary diversion specific impact on bladder cancer recurrence
From enrollment to late follow-up, up to 7 years
Number of participants who will die from bladder cancer according to Urinary diversions
Tidsramme: From enrollment to late follow-up, up to 7 years
Urinary diversion specific impact on bladder cancer rmortality
From enrollment to late follow-up, up to 7 years
Number of participants who will die from all causes according to Urinary diversions
Tidsramme: From enrollment to late follow-up, up to 7 years
Urinary diversion specific impact on all cause mortality after surgery
From enrollment to late follow-up, up to 7 years

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Arcangelo Sebastianelli, MD, Careggi Hospital, University of Florence
  • Hovedetterforsker: Simone Morselli, MD, University of Florence

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

29. april 2021

Primær fullføring (Forventet)

1. februar 2031

Studiet fullført (Forventet)

1. februar 2038

Datoer for studieregistrering

Først innsendt

3. mai 2021

Først innsendt som oppfylte QC-kriteriene

19. mai 2021

Først lagt ut (Faktiske)

25. mai 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

25. mai 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

19. mai 2021

Sist bekreftet

1. mai 2021

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere