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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03767166
Other study ID # 2275
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2019
Est. completion date December 31, 2020

Study information

Verified date March 2021
Source Istituto Clinico Humanitas
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a prospective, phase II, single-centre, non-randomised, single-arm study, enrolling patients with benign and malignant bilio-pancreatic diseases with an indication to biliary or pancreatic plastic stent positioning during ERCP. On procedure day, the study team will confirm that the patient meets all the inclusion criteria and none of the exclusion criteria. The patient will undergo the ABS insertion and monitored and follow-up accordingly to biodegration variant.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with an indication to position one ore more biliary plastic stents during ERCP - Patients with an indication to position a pancreatic plastic stent during ERCP Exclusion Criteria: - Age < 18 y - Life expectancy < 1 m, - Inability to pass a guidewire through stricture - Contra-indication for endoscopy or interventional radiology - Presence of partial gastric resection - Unsigned informing consent form, ICF - Pregnancy - Pseudo Klatskin tumors (metastases in the liver hilum) and gallbladder carcinoma

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Biodegradable biliary and pancreatic stents placement
Biodegradable biliary and pancreatic stents placement

Locations

Country Name City State
Italy Endoscopy Unit, Humanitas Research Hospital Rozzano Milano

Sponsors (1)

Lead Sponsor Collaborator
Istituto Clinico Humanitas

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Biodegradation time 24 Months
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