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Impact of Suction in the EUS-guided Fine Needle Biopsy of Solid Pancreatic Lesions

Primary Purpose

Biopsy, Fine-Needle, Endosonography, Pancreatic Neoplasm

Status
Unknown status
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
EUS-guided FNB with Syringe Suction
EUS-guided FNB without Syringe Suction
Sponsored by
Centro Hospitalar De São João, E.P.E.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Biopsy, Fine-Needle

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with 18 years of age and older;
  • Ability to provide free and informed consent before entering the study;
  • Imaging diagnosis of a solid pancreatic lesion that was proposed for EUS characterization;
  • Presence of sectional imaging method (CT/MRI) performed within six months before randomization;
  • Blood test (blood count and coagulation studies) compatible with the performance of invasive maneuvers;
  • Clinical indication by the endoscopist for EUS-tissue acquisition with the use of an FNB needle.

Exclusion Criteria:

  • Failure to provide free and informed consent;
  • Clinically significant change in haemostasis laboratory parameters: International Normalized Ratio (INR) > 1.5; activated partial thromboplastin time (aPTT)> 50 seconds; Platelets <50,000;
  • Absence of a proper anticoagulant and/or anti-aggregate therapy discontinuation for the performance of FNB;
  • Absence of fasting (2h without clear liquids and 6h without solid foods);
  • Clinical suspicion of upper digestive tract obstruction;
  • An episode of acute pancreatitis within four weeks before echoendoscopy;
  • Respiratory failure or hemodynamic instability;
  • Pregnancy or breast-feeding.

Sites / Locations

  • Centro Hospitalar São JoãoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

EUS-guided FNB with syringe suction

EUS-guided FNB without syringe suction

Arm Description

Outcomes

Primary Outcome Measures

Diagnostic Yield
Percentage of the lesions sampled for which a tissue diagnosis is obtained and specimen adequacy is defined as the percentage of lesions sampled in which the obtained material is representative of the target site and sufficient for diagnosis
Accuracy
Percentage of lesions sampled by EUS-tissue aquisition techniques that correspond to the final diagnosis at surgical histopathology or clinical follow-up (at least 12 months) for patients with nondiagnostic sampling.

Secondary Outcome Measures

Full Information

First Posted
November 12, 2019
Last Updated
November 13, 2019
Sponsor
Centro Hospitalar De São João, E.P.E.
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1. Study Identification

Unique Protocol Identification Number
NCT04164017
Brief Title
Impact of Suction in the EUS-guided Fine Needle Biopsy of Solid Pancreatic Lesions
Official Title
Comparative Evaluation of the Diagnostic Yield and Sample Quality in Endoscopic Ultrasound(EUS)-Guided Fine Needle Biopsy(FNB) of Pancreatic Solid Lesions With and Without Syringe Suction
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2019 (Actual)
Primary Completion Date
April 1, 2020 (Anticipated)
Study Completion Date
April 1, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Hospitalar De São João, E.P.E.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Tissue acquisition by Endoscopic Ultrasound (EUS) has become a modality of diagnosis and clinical orientation for several diseases. Although tissue acquisition traditionally involves the cytological diagnosis (using fine-needle aspiration/FNA), the importance of obtaining a core for histological examination (by fine-needle biopsy/FNB) has recently been recognized. Currently, there is no clear establishment of the usefulness of syringe suction for the diagnostic accuracy of solid pancreatic lesions when FNB is used. Because of that, the investigators aimed to compare sensitivity, sample adequacy, and diagnostic yield of solid pancreatic lesions EUS-guided sampling using with and without syringe suction. The study will be conducted on a consecutive sample of patients proposed to perform EUS for solid pancreatic lesions characterization, in which the clinical and imaging findings justify the need for an FNB. For each case, FNB will be performed using two punctures: one with 20mL syringe suction, and another without suction. The order in which they will be performed will be known only by the performing physician and the nursing team at the time that FNB is proposed. This information will be concealed from the pathologist responsible for sample analysis. Clinical care during and after the procedure will follow the existing guidelines. Participants will undergo a single clinical evaluation (at the time of endoscopy and recovery) without the need for follow-up visits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Biopsy, Fine-Needle, Endosonography, Pancreatic Neoplasm

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
EUS-guided FNB with syringe suction
Arm Type
Experimental
Arm Title
EUS-guided FNB without syringe suction
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
EUS-guided FNB with Syringe Suction
Intervention Description
For each case, FNB will be performed using two punctures: one with 20mL syringe suction and another without aspiration. The order in which they will be performed will be known only by the performing physician and the nursing team at the time that FNB is proposed. This information will be concealed from the pathologist responsible for sample analysis.
Intervention Type
Device
Intervention Name(s)
EUS-guided FNB without Syringe Suction
Intervention Description
For each case, FNB will be performed using two punctures: one with 20mL syringe suction and another without aspiration. The order in which they will be performed will be known only by the performing physician and the nursing team at the time that FNB is proposed. This information will be concealed from the pathologist responsible for sample analysis.
Primary Outcome Measure Information:
Title
Diagnostic Yield
Description
Percentage of the lesions sampled for which a tissue diagnosis is obtained and specimen adequacy is defined as the percentage of lesions sampled in which the obtained material is representative of the target site and sufficient for diagnosis
Time Frame
Through study completion, an average of 10 months
Title
Accuracy
Description
Percentage of lesions sampled by EUS-tissue aquisition techniques that correspond to the final diagnosis at surgical histopathology or clinical follow-up (at least 12 months) for patients with nondiagnostic sampling.
Time Frame
Through study completion, an average of 10 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with 18 years of age and older; Ability to provide free and informed consent before entering the study; Imaging diagnosis of a solid pancreatic lesion that was proposed for EUS characterization; Presence of sectional imaging method (CT/MRI) performed within six months before randomization; Blood test (blood count and coagulation studies) compatible with the performance of invasive maneuvers; Clinical indication by the endoscopist for EUS-tissue acquisition with the use of an FNB needle. Exclusion Criteria: Failure to provide free and informed consent; Clinically significant change in haemostasis laboratory parameters: International Normalized Ratio (INR) > 1.5; activated partial thromboplastin time (aPTT)> 50 seconds; Platelets <50,000; Absence of a proper anticoagulant and/or anti-aggregate therapy discontinuation for the performance of FNB; Absence of fasting (2h without clear liquids and 6h without solid foods); Clinical suspicion of upper digestive tract obstruction; An episode of acute pancreatitis within four weeks before echoendoscopy; Respiratory failure or hemodynamic instability; Pregnancy or breast-feeding.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pedro Costa-Moreira
Phone
+351913543173
Email
pedromoreira.med@gmail.com
Facility Information:
Facility Name
Centro Hospitalar São João
City
Porto
ZIP/Postal Code
4200-319
Country
Portugal
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pedro Costa-Moreira
Phone
+351913543173
Email
pedromoreira.med@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29074447
Citation
Wani S, Muthusamy VR, McGrath CM, Sepulveda AR, Das A, Messersmith W, Kochman ML, Shah J. AGA White Paper: Optimizing Endoscopic Ultrasound-Guided Tissue Acquisition and Future Directions. Clin Gastroenterol Hepatol. 2018 Mar;16(3):318-327. doi: 10.1016/j.cgh.2017.10.020. Epub 2017 Oct 23. No abstract available.
Results Reference
background
PubMed Identifier
25434654
Citation
Wani S, Muthusamy VR, Komanduri S. EUS-guided tissue acquisition: an evidence-based approach (with videos). Gastrointest Endosc. 2014 Dec;80(6):939-59.e7. doi: 10.1016/j.gie.2014.07.066. No abstract available.
Results Reference
background
PubMed Identifier
26430767
Citation
Dwyer J, Pantanowitz L, Ohori NP, Pai RK, Vrbin C, Brand RE, Monaco SE. Endoscopic ultrasound-guided FNA and ProCore biopsy in sampling pancreatic and intra-abdominal masses. Cancer Cytopathol. 2016 Feb;124(2):110-21. doi: 10.1002/cncy.21623. Epub 2015 Oct 2.
Results Reference
background
PubMed Identifier
23433878
Citation
Lee JK, Choi JH, Lee KH, Kim KM, Shin JU, Lee JK, Lee KT, Jang KT. A prospective, comparative trial to optimize sampling techniques in EUS-guided FNA of solid pancreatic masses. Gastrointest Endosc. 2013 May;77(5):745-51. doi: 10.1016/j.gie.2012.12.009. Epub 2013 Feb 21.
Results Reference
background
PubMed Identifier
11577304
Citation
Wallace MB, Kennedy T, Durkalski V, Eloubeidi MA, Etamad R, Matsuda K, Lewin D, Van Velse A, Hennesey W, Hawes RH, Hoffman BJ. Randomized controlled trial of EUS-guided fine needle aspiration techniques for the detection of malignant lymphadenopathy. Gastrointest Endosc. 2001 Oct;54(4):441-7. doi: 10.1067/mge.2001.117764.
Results Reference
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Impact of Suction in the EUS-guided Fine Needle Biopsy of Solid Pancreatic Lesions

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