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Pancreatic MassesNCT07032974

RCT Comparing Accuracy Among Franseen, Forward-bevel Westcott, and Fork-tip EUS-FNB Needle in Diagnosis of Solid Pancreatic Lesions

A study testing Franseen, Forward-bevel and Fork-tip in people with Pancreatic Masses, run by Mahidol University at 1 site in Thailand.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Endoscopic Ultrasound-Guided Fine Needle Aspiration (EUS-FNA) is a well-established technique for pancreatic tissue acquisition, offering a high diagnostic accuracy ranging from 78% to 95%, along with a favorable safety profile. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pancreatic Masses
What is being tested?
Franseen, Forward-bevel and Fork-tip
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
108 participants
Where
1 siteThailand
Study dates
1 Jul 2025to Jul 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age > 18 years
  • Solid pancreatic mass greater than 1 cm in size who required tissue diagnosis

Who cannot join

  • Pregnancy
  • Uncorrected coagulopathy
  • Surgically altered anatomy
  • Unable to complete informed consent

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Ronnakorn Kongsakon, MD contact

+66655979522

ronnagorn@gmail.com

Thailand1 site, 1 recruiting
  • Faculty of Medicine Siriraj Hospital, Mahidol University

    Bangkok, Bangkok, 10700

    Ronnakorn Kongsakon, MD, +66655979522, ronnagorn@gmail.com

    Recruiting

Other trials in Thailand

About this study

Official title: Prospective Randomized Controlled Trial Comparing Accuracy Among Franseen, Forward-bevel Westcott, and Fork-tip Needle Design for EUS-guided Fine Needle Biopsy in Diagnosis of Solid Pancreatic Lesions

Endoscopic Ultrasound-Guided Fine Needle Aspiration (EUS-FNA) is a well-established technique for pancreatic tissue acquisition, offering a high diagnostic accuracy ranging from 78% to 95%, along with a favorable safety profile. Over time, numerous studies have sought to optimize this procedure by investigating various contributing factors, including needle size, sampling techniques, adequacy of tissue acquisition, the number of passes required, and needle type. These insights have largely been incorporated into routine clinical practice, refining the diagnostic capabilities of EUS-FNA.

Despite its widespread use, EUS-FNA has limitations, particularly in the diagnosis of certain pancreatic pathologies such as lymphoma, gastrointestinal stromal tumors (GISTs), and autoimmune pancreatitis. These conditions often require histologic samples for ancillary studies, which cytologic specimens obtained via FNA cannot sufficiently provide. To overcome this limitation, Fine Needle Biopsy (FNB) needles were developed. These needles enable the procurement of core tissue samples, thereby enhancing histopathological assessment and reducing reliance on rapid on-site cytological evaluation (ROSE). Additionally, FNB allows for fewer needle passes, which can shorten procedure time and reduce associated complications.

Read more

Among FNB technologies, the third generation of needles has garnered particular attention due to improved sample adequacy and diagnostic reliability. While earlier research compared second-generation FNB needles with FNA, demonstrating no significant difference in diagnostic yield, more recent studies suggest that third-generation FNB needles offer superior diagnostic accuracy.

Currently, three distinct third-generation FNB needle types are commercially available, distinguished by their tip geometry:

Franseen geometry - Acquire™ (Boston Scientific)

Fork-tip - SharkCore™ (Medtronic)

Forward-bevel Westcott - ProCore™ (Cook Medical)

Despite their clinical adoption, comparative data on their diagnostic performance remain scarce. Only two randomized controlled trials (RCTs) have directly compared these needle types:

Karsenti et al. compared the Franseen (Acquire) and the Forward-bevel Westcott (ProCore) needles for pancreatic mass diagnosis. Diagnostic accuracy was 87% (CI: 75-94) for the Franseen needle and 67% (CI: 53-78) for the Westcott needle, with a statistically significant difference (p = 0.02).

Ashat et al. evaluated the Franseen (Acquire) and Fork-tip (SharkCore) needles in diagnosing all gastrointestinal masses, reporting diagnostic accuracies of 85.3% and 90.7%, respectively (p = 0.45). In a pancreatic mass-specific subgroup analysis, accuracy rates were 89.7% and 94.4%, respectively (p = 0.68), suggesting comparable performance between the two.

Despite these findings, the current literature does not include a comprehensive head-to-head comparison encompassing all three third-generation FNB needle types. Therefore, it remains uncertain which design offers the best diagnostic performance for pancreatic tumors. The absence of such comparative studies presents a significant gap in the field of EUS-guided tissue acquisition.

Read the detailed description

Endoscopic Ultrasound-Guided Fine Needle Aspiration (EUS-FNA) for pancreatic tissue acquisition is a widely accepted and popularly used technique because of its high diagnostic accuracy of 78% - 95% and a low risk of adverse events.

Previous studies have tried to identify ways to increase the efficacy and diagnostic accuracy of EUS-FNA. Many factors were found to influence the diagnostic accuracy of EUS-FNA which included needle size, sampling technique, evaluation of tissue adequacy, number of needle passes, and finally the needle type, which the impact of most of the aforementioned factors were thoroughly studied and already incorporated into the standard practice of pancreatic tissue acquisition.

It was difficult to diagnose some pancreatic diseases by EUS-FNA, such as lymphoma, gastrointestinal stromal tumor (GIST), and autoimmune pancreatitis because the cytologic specimen was simply not enough for further ancillary studies. FNB needles were subsequently developed to eliminate this limitation, by obtaining a larger specimen, FNB needles enable pathologists to evaluate the specimens more thoroughly and help guide further therapeutic decisions. In addition, it reduces the dependency on immediate cytological examination during endoscopy (Rapid on-site evaluation [ROSE]) and also reduces the procedure duration, since the number of needle passes is reduced.

The continuous development of EUS-FNB needles has been a major area of interest in recent years. In particular, the third generation of FNB needles were developed to obtain a more adequate tissue sample. Previous research has focused on comparing the accuracy of the second generation FNB needles with the FNA needles in the diagnosis of pancreatic tissue. Results from these studies found no significant differences between the two needles. However, it was discovered that the third generation FNB needle has significantly higher diagnostic accuracy than the FNA needle. These findings suggest that the third generation FNB needle may be a more reliable and effective tool for diagnosing tissue samples in various clinical settings.

In the field of tissue biopsy, the third generation FNB needle is currently available in three types based on the characteristics of the needle tip. These types include Franseen geometry needle (Acquire, Boston Scientific), Fork-tip needle (Shark-core, Medtronic), and Forward-bevel Westcott (Procore, Cook Medical). However, there is a lack of research comparing the diagnostic accuracy of among each type of needle. Only two randomized controlled trials have been conducted to address this issue. Karsenti et al. investigated the accuracy of diagnosing a pancreatic mass using Franseen geometry needle (Acquire, Boston Scientific) and Forward-bevel Westcott (Procore, Cook Medical). The study found accuracy rates of 87% (75-94) and 67% (53-78), respectively, with a p-value of 0.02. Ashat et al. compared the accuracy of diagnosing all gastrointestinal masses using Franseen geometry needle (Acquire, Boston Scientific) and Fork-tip needle (Shark-core, Medtronic), finding accuracy rates of 85.3% and 90.7%, respectively, with a p-value of 0.45. Subgroup analysis for pancreatic masses alone found accuracy rates of 89.7% and 94.4%, respectively, with a p-value of 0.68.

In the context of diagnosing pancreatic tissue masses, only a limited number of studies have examined the comparative accuracy of 3rd generation fine needle biopsy (FNB) needles. As such, it remains unclear which type of needle can deliver superior diagnostic precision, and to date, no study has conducted a head-to-head comparison of all three needle types. Thus, the purpose of the present investigation is to assess the diagnostic accuracy of all three 3rd generation FNB needle types in the context of detecting pancreatic tumors.

Being tested
Franseen, Forward-bevel, Fork-tip
Keywords
Pancreatic mass, EUS, EUS-FNB, Fine needle biopsy, Endoscopic ultrasound, Pancreatic lesion

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • FranseenDevice

    Franseen needle

  • Forward-bevelDevice

    Forward-bevel needle

  • Fork-tipDevice

    Fork-tip needle

Study groups in NCT07032974
Study groupRoleWhat they receive
FranseenExperimentalNot described
Receives: Device: Franseen
Forward- bevelExperimentalNot described
Receives: Device: Forward-bevel
Fork-tipExperimentalNot described
Receives: Device: Fork-tip

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Diagnostic accuracy

    Diagnostic accuracy of three third-generation fine-needle biopsy (FNB) needles

    Measured: 6 months

Secondary outcomes (4)
  1. Number of needle passes

    Number of needle passes during EUS

    Measured: During procedure

  2. Overall satisfaction

    Overall satisfaction of endoscopist during EUS including needle visiblity, maneuverability and ease of puncture on a scale of 0 to 2.

    Measured: During procedure

  3. Procedure time

    Procedure time of EUS

    Measured: During procedure

  4. Adverse events

    Adverse events of the procedure

    Measured: up to 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2025
  2. Study start1 Jul 2025 (estimated)
  3. Primary completionJul 2026 (estimated)
  4. Study completionJul 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
108 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07032974
Sponsor's protocol ID
Si 316/2022
Status last verified
Mar 2025
First submitted
12 Jun 2025
Last updated
24 Jun 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: We are willing to provide our data to researchers who require it. For example, those who want to do systematic review and meta-analysis.

Questions about this trial

What is this clinical trial studying?

A study testing Franseen, Forward-bevel and Fork-tip in people with Pancreatic Masses, run by Mahidol University at 1 site in Thailand.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 24 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Thailand. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Ronnakorn Kongsakon, MD (+66655979522, ronnagorn@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Diagnostic accuracy (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2025.

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