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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
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pancreatic Neoplasms

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
December 5, 2018
Last Updated
February 9, 2023
Sponsor
Chinese University of Hong Kong
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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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