EUS-FNB With MOSE vs EUS-FNA With ROSE (MORE)
Primary Purpose
Pancreatic Neoplasms
Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
MOSE
ROSE
Sponsored by
About this trial
This is an interventional diagnostic trial for Pancreatic Neoplasms
Eligibility Criteria
Inclusion Criteria:
- Aged between 18 and 80 years
- Referred for EUS-guided tissue acquisition of solid pancreatic lesions greater than 1cm in the largest diameter
Exclusion Criteria:
- Coagulopathy
- Altered anatomy
- Contraindications for conscious sedation
- Pregnancy
- Those who cannot provide informed consent
Sites / Locations
- Department of Surgery; The Chinese University of Hong KongRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
MOSE
ROSE
Arm Description
EUS-FNB with MOSE
EUS-FNA with ROSE
Outcomes
Primary Outcome Measures
Diagnostic yield
the proportion of patients with adequate tissue for diagnosis
Secondary Outcome Measures
morbidity rate
Procedure-related morbidity
Full Information
NCT ID
NCT03766659
First Posted
December 5, 2018
Last Updated
February 9, 2023
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT03766659
Brief Title
EUS-FNB With MOSE vs EUS-FNA With ROSE
Acronym
MORE
Official Title
Endoscopic Ultrasound-guided Fine Needle Biopsy With Macroscopic On-Site Evaluation vs Fine Needle Aspiration With Rapid On-Site Evaluation for Solid Pancreatic Lesions: A Multi-centered Prospective Randomized Controlled Trial (MORE Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 19, 2019 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
September 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) is an indispensable tool for tissue acquisition for pancreatic lesions. However, FNA alone has several limitations including inadequate acquisition of cells, and unable to provide core tissue for further histological analysis. The use of rapid on-site evaluation (ROSE) by cytopathologist has the biggest impact on improving diagnostic accuracy and is regarded as the gold standard for EUS-FNA. Unfortunately, it is not widely available due to limited resources.
In order to overcome these limitations, new fine needle biopsy (FNB) needles have been recently developed to collect not only cells but also the entire core tissue for histological analysis. Having core biopsy with preserved tissue provides additional advantages of allowing molecular analysis, which are of emerging importance in cancer management. Early results comparing FNB with FNA showed the superiority of FNB over FNA in the absence of ROSE. Data comparing FNB and FNA with ROSE are limited. In order to study to true merits of FNB over FNA, comparison with the most optimal method is necessary.
Detailed Description
The purpose of this study is to compare the diagnostic yield of EUS-FNB with MOSE vs EUS-FNA with ROSE.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Neoplasms
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
International multicenter prospective randomized comparative study.
Masking
Participant
Allocation
Randomized
Enrollment
340 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MOSE
Arm Type
Other
Arm Description
EUS-FNB with MOSE
Arm Title
ROSE
Arm Type
Other
Arm Description
EUS-FNA with ROSE
Intervention Type
Diagnostic Test
Intervention Name(s)
MOSE
Intervention Description
EUS-FNB with MOSE
Intervention Type
Diagnostic Test
Intervention Name(s)
ROSE
Intervention Description
EUS-FNA with ROSE
Primary Outcome Measure Information:
Title
Diagnostic yield
Description
the proportion of patients with adequate tissue for diagnosis
Time Frame
1 month after Procedure
Secondary Outcome Measure Information:
Title
morbidity rate
Description
Procedure-related morbidity
Time Frame
1 month after Procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged between 18 and 80 years
Referred for EUS-guided tissue acquisition of solid pancreatic lesions greater than 1cm in the largest diameter
Exclusion Criteria:
Coagulopathy
Altered anatomy
Contraindications for conscious sedation
Pregnancy
Those who cannot provide informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Charing CHONG
Phone
3505 3933
Email
chongcn@surgery.cuhk.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Philip Yeung
Phone
3404 3933
Email
philipyeung@surgery.cuhk.edu.hk
Facility Information:
Facility Name
Department of Surgery; The Chinese University of Hong Kong
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Charing C Chong, MBChB
Phone
852-26321496
Email
Chongcn@surgery.cuhk.edu.hk
First Name & Middle Initial & Last Name & Degree
Charing C Chong, MBChB
12. IPD Sharing Statement
Learn more about this trial
EUS-FNB With MOSE vs EUS-FNA With ROSE
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