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Moray Micro Forceps and Pancreatic Cyst (MOBIDYC)

V

VANBIERVLIET

Status

Unknown

Conditions

Pancreas Cyst

Treatments

Diagnostic Test: Biopsy of the cyst wall with the Moray™ forceps.

Study type

Interventional

Funder types

Other

Identifiers

NCT04200131
SFED N 133

Details and patient eligibility

About

The prevalence of pancreatic cysts in the general population is high close to 1%. The diagnosis is most of the time fortuitous thanks to the improvement of the imaging resources available. These lesions include a large number of entities, some of with malignant potential. Mucinous lesions present a high risk of tumor transformation, justifying surgery, which is sometimes heavy. It appears essential to select the best patients to benefit from this type of treatment. For this purpose, the accuracy of the diagnostic means must be optimal. The Fine Needle Aspiration under Endoscopic ultrasound, validated in this context, have a low complication rate. It allows a cytological evaluation and analysis of tumor markers measurements in cystic fluid. However, cytopathological evaluation is only contributing in 1/3 to half of cases. The assays of markers (including the main one ACE) have high specificities but high insufficient sensitivities (less than 50%). Molecular techniques (K-RAS mutation in particular), of variable availability, allow to increase the sensitivity in association with the other diagnostic parameters. But the rate of false negatives remains above 20% to date. A diagnostic means to obtain a histology of the cyst wall would reduce considerably the risk of error.

The Moray™ micro forceps is forceps that aims to provide a tissue sample of the wall of the pancreatic cyst. It is inserted into a commonly used 19 Gauge needle during the puncture of the cyst under endoscopic ultrasound. It could increase the accuracy diagnosis of the procedure. These forceps has recently become available to the practitioner and has obtained the CE marking.

To date, no quality multi-center prospective evaluation has determined the capacity of to obtain a histology of the pancreatic cystic walls by this technique. Its safety must be also be accurately assessed.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age over 18 years old
  • FNA of the cystic fluid indicated during an endoscopic ultrasound examination
  • Abdominal CT and pancreatic MRI less than 3 months old, available
  • Pancreatic cyst unilocular or with a macrolocule in case of multilocular cyst, of size ≥ to 20 mm of major axis with a clean wall.

Exclusion criteria

  • Contraindication to performing an upper endoscopic ultrasound
  • Patient with known chronic calcifying pancreatitis, or suspected on the iconography available during the screening visit
  • Patient taking an antiplatelet, or anticoagulant therapy including anti-vitamin K, direct oral anticoagulant, or heparin.
  • Hemorrhagic disease, hemostasis and coagulation disorder (TP < 60%, TCA > 40 sec. and platelets < 60000/mm3), malignant hematopathy, chronic cirrhotic liver disease with Child Pugh B or C, acute or severe chronic renal failure (creatinine clearance < to 30 ml/min)
  • Mental disability of the subject making participation in the trial impossible
  • Patient not affiliated to a social security system
  • Inability to understand or sign informed consent
  • Serious adverse events
  • Early termination of participation, withdrawal of voluntary informed consent of the patient
  • Violation of protocol

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Moray micro-forceps
Experimental group
Treatment:
Diagnostic Test: Biopsy of the cyst wall with the Moray™ forceps.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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