Percutaneous Transluminal Forceps Biopsy

NCT06039670 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2023-09-15

No results posted yet for this study

Summary

To evaluate during a 7 months period the efficacy, safety and accuracy of percutaneous transluminal forceps biopsy combined with transhepatic biliary drainage in patients with biliary stricture

Conditions

  • Biliary Stricture
  • Biopsy Wound
  • Oncology

Interventions

PROCEDURE

biliary biopsy

biliary biopsy through a percutaneous approach during a percutaneous biliary drainage

Sponsors & Collaborators

  • University Hospital, Caen

    lead OTHER

Principal Investigators

  • Audrey Fohlen · Caen UH

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-02
Primary Completion
2015-07-31
Completion
2016-08-31

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06039670 on ClinicalTrials.gov