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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03807687
Other study ID # PAD-R 1101CESC
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2016
Est. completion date December 1, 2046

Study information

Verified date January 2019
Source Azienda Ospedaliera Universitaria Integrata Verona
Contact Erica Secchettin
Phone +390458126254
Email erica.secchettin@aovr.veneto.it
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This clinical data registry records information about the health status and healthcare performances received by participants affected by every type of pancreatic disease or disorder. All data (demographic, clinical, biochemical, radiological, pharmacological, genetic...) and audio and/or video recording from operative room are collected in order to be used for prospective or retrospective studies.


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date December 1, 2046
Est. primary completion date December 1, 2046
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- any type of pancreatic disease: inflammatory and neoplastic (including solid and cystic lesions)

Exclusion Criteria:

- physically or mentally inability to provide consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy AOUI Verona Verona

Sponsors (1)

Lead Sponsor Collaborator
Azienda Ospedaliera Universitaria Integrata Verona

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival Survival from Diagnosis to time of death 1 year
Secondary Postoperative morbidity Occurrence of Pancreatic Fistula, Biliary fistula, Enteric fistula, Delayed Gastric Emptying, Hemorrhage or Sepsis. 90 days
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