- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04900558
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
Status
Rekruttering
Intervensjon / Behandling
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
- Navn: Simone Morselli, MD
- Telefonnummer: 3473050852
- E-post: simone.morselli.89@gmail.com
Studer Kontakt Backup
- Navn: Silvia Benemei, PhD
- E-post: silvia.benemei@unifi.it
Studiesteder
-
-
Tuscany
-
Florence, Tuscany, Italia, 50134
- Rekruttering
- Careggi University Hospital
-
Underetterforsker:
- Mauro Gacci, MD
-
Underetterforsker:
- Riccardo Campi, MD
-
Ta kontakt med:
- Arcangelo Sebastianelli, MD
- E-post: arcangelo.sebastianelli@gmail.com
-
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.
Sponsor
Samarbeidspartnere
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
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 19303_oss
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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