Percutaneous Transluminal Forceps Biopsy

C

Caen University Hospital

Status

Completed

Conditions

Oncology
Biliary Stricture
Biopsy Wound

Treatments

Procedure: biliary biopsy

Study type

Observational

Funder types

Other

Identifiers

NCT06039670
PTFB

Details and patient eligibility

About

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

Full description

Biological parameters of liver function, histopathology of specimens, comparison with others clinical and pathological data (imaging follow up, percutaneous biopsy, surgical biopsy, endoscopic biopsy) were recorded Comparison between pathological findings of surgery or endoscopy or percutaneous biopsy and specimens coming from biliary forceps biopsy follow up of the patient 12 months after biopsy Evaluation of complications, accuracy

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with biliary strictures without histology available

Exclusion criteria

  • Pregnant patients
  • Children

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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