Intermittent Suction Technique in the Diagnosis of Pancreatic Solid Lesions

Sponsor
Fundación de Investigación Biomédica - Hospital Universitario de La Princesa (Other)
Overall Status
Completed
CT.gov ID
NCT03829748
Collaborator
(none)
33
1
2
13.5
2.4

Study Details

Study Description

Brief Summary

The aim of this study is to compare the diagnostic yield of intermittent versus continuous suction in the diagnosis of pancreatic solid lesions.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Intermittent aspiration
N/A

Detailed Description

Solid lesions of the pancreas can be neoplastic or non neoplastic and it is important to accurately differentiate between them because of the poor prognosis related to pancreatic neoplasm. There are many types of solid pancreatic lesions: pancreatic adenocarcinoma, neuroendocrine tumor, lymphoma, solid pseudopapillary neoplasm and pancreatic metastasis.

There are several diagnostic methods for the study of pancreatic solid lesions. The different imaging test allow detection and characterization of those lesions, but most times an anatomopathological diagnosis is needed before stablishing the most appropriate treatment.

Endoscopic Ultrasound guided fine needle aspiration (EUS-FNA) is the diagnostic method of choice for the diagnosis of these lesions as it detects small lesions that sometimes cannot be found in radiological imaging test, evaluates vascular invasion and the presence of liver metastasis, and allows pancreatic puncture for a cytological diagnosis. EUS-FNA is the safest technique for pancreatic puncture and the least related to needle track seeding.

In order to gather as much material as possible different techniques have been proposed:
  • Fanning technique and multiple pass technique: to guide the needle into different regions of the target lesions with or without removing the needle out of the lesion depending on wether the lesion is hard or soft.

  • Use of stylet: there are no data clearly demonstrating that the use of suction increases the yield of EUS-FNA. Some authors do slow withdrawal of the stylet.

  • Size of the needle: 19 gauge, 22 gauge, 25 gauge, depending on the localization, size and vascularization. There is increasing evidence that smaller needles offer at least similar results in diagnostic yield compared to larger needles and are also easier to manipulate.

  • Use of suction: there is conflicting evidence in this point. Several studies have evaluated the use of high volume aspiration vs low volume aspiration, continous aspiration vs no aspiration and suction with empty syringe vs water-filled syringe but none is clearly better than other.

The investigators aim is to evaluate if the use of intermittent suction improves the diagnostic yield of pancreatic lesions compared to standard (continuous) suction. Up to our knowledge this method has not been yet evaluated.

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
Intermittent Versus Continuous Suction Technique in the Diagnosis of Pancreatic Solid Lesions. A Pilot Study.
Actual Study Start Date :
Jan 16, 2019
Actual Primary Completion Date :
Jan 16, 2020
Actual Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intermittent aspiration

Empty syringe of 10cc and intermittent aspiration during puncture

Procedure: Intermittent aspiration
Endoscopic ultrasound is done for the localization of the lesion and to localize the site of puncture.Prior to the puncture of the lesion the stylet is removed and a vacuum syringe is prepared with 10 cc of vacuum allowing the generation of continous pressure inside and connected to the end of the needle. Once the lesion is punctured 15 movements in and out of the lesions will be made while the syringe is opened and closed on and off for a total of 3 times each pass. A total of 4 passes will be done in each lesion.

No Intervention: Continous/standard aspiration

Empty syringe of 10cc and continous aspiration during puncture

Outcome Measures

Primary Outcome Measures

  1. Increase in diagnostic yield of pancreatic solid lesions [Baseline]

    Percentage of increase in positive smears between intermittent and continous suction

Secondary Outcome Measures

  1. Sample cellularity [Baseline]

    Number of malignant clusters of cells on each endoscopic pass

  2. Blood contamination [Baseline]

    Percentage of blood contamination of the slides

  3. Number of passes to reach diagnosis [Baseline]

    Number of passes needed to achieve a positive cytological diagnosis

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Pancreatic solid lesion

  • Patients over 18 years old

  • Suitable for endoscopy

Exclusion Criteria:
  • Contraindication for endoscopy

  • Active anticoagulant therapy

  • Thrombocytopenia or coagulopathy in the absence of its correction prior to the procedure

  • Absence of informed consent

  • Pregnancy

  • Not accessible lesion for endoscopic ultrasound puncture

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Universitario de la Princesa Madrid Spain 28006

Sponsors and Collaborators

  • Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

Investigators

  • Principal Investigator: Herranz Pérez, MD, Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Fundación de Investigación Biomédica - Hospital Universitario de La Princesa
ClinicalTrials.gov Identifier:
NCT03829748
Other Study ID Numbers:
  • RHerranz3638
First Posted:
Feb 4, 2019
Last Update Posted:
May 22, 2020
Last Verified:
May 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Fundación de Investigación Biomédica - Hospital Universitario de La Princesa
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 22, 2020