Moray Micro Forceps and Pancreatic Cyst

Pancreas Cyst Clinical Trial

— MOBIDYC  

Official title:

Histological Diagnostic Value of the Moray Micro Forceps in the Management of Pancreatic Cysts.

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04200131
• Other study ID #: SFED N 133
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 22, 2020
• Est. completion date: March 2023

Study information

• Verified date: May 2022
• Source: Société Française d'Endoscopie Digestive
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 100
• Est. completion date: March 2023
• Est. primary completion date: July 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Cysts
• Pancreas Cyst
• Pancreatic Cyst

Intervention

Diagnostic Test:
• Biopsy of the cyst wall with the Moray™ forceps.
Tissue sample of the wall of the pancreatic cyst with micro Moray™ forceps during an ultrasound-guided puncture of a pancreatic cyst with a 19G needle.

Locations

Country	Name	City	State
France	University hospital of Archet II	Nice

Sponsors (1)

Lead Sponsor	Collaborator
VANBIERVLIET

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Obtaining histological diagnosis by using "The Moray" micro forceps.	Obtaining enough tissue material by using "The Moray" micro forceps allowing paraffin embedding, histological analysis and diagnosis according to the opinion of the pathologist. The ability of the micro-forceps to obtain a positive sample will be determined histologically. The proportion % of the positive samples (diagnosis from the pathologist) will correspond to the number of patients whose histological diagnosis is obtained according to the pathologist (tissue with presence of a chorion / extracellular matrix) divided by the total number of patients enrolled in this trial.	Day 10
Secondary	The diagnostic accuracy of the technique (The Moray" micro forceps)	The diagnostic accuracy of the technique will be determinate by comparison between the results obtained after using the Moray micro forceps and diagnosis retained after surgery. If the surgery is not performed, the diagnostic accuracy will be determined by 3 independent experts by using the morphological results of the different iconographies, cytology, intracystic fluid dosages	6 months
Secondary	Emergent Adverse Events of the technique (the Moray micro-forceps)	The emergent adverse events will be assessed (Moray micro forceps) by compilation of all adverse events occurring immediately or at 30 days post-procedure (hemorrhages, possible episodes of acute pancreatitis or infection) according to degree of the severity: slight, moderate, severity, and fatal( cotton's criterions).The proportion of patients presenting at least one morbid event during the biopsy and after post-procedure (immediately) will be calculated and compared by using Prescott test. In the same way, the delayed morbidity of the procedure as a whole will be described by the proportion of patients who had a morbid event delayed between the end of the procedure and Day 30.	Day 0 and after 1 month
Secondary	Technical success of the Moray micro-forceps	Assessed by the proportion of patients whose procedure allow obtained a biopsy in absence of a technical incident: passage of the micro-forceps through the 19G needle, its opening, the acquisition of tissue material, and its removal from the needle at the end of the procedure.	Day 0
Secondary	Satisfaction of the technique (Moray micro-forceps) on the management of pancreatic cyst	Estimated by the proportion of patients for which the decision by the monitoring experts was different after obtaining the result of the samples by the Moray micro-forceps compared to a usual support based on the techniques available today.	6 months
Secondary	Quality of the sample	Determined by the proportion of samples with a histological analyzable surface by the pathologist.	Day 10