An RCT of 19G EBUS-TBNA Needle in Suspected Sarcoidosis

Sarcoidosis Clinical Trial

— GUESS  

Official title:

A Study Evaluating the Diagnostic Yield and Safety of the 19-GaUge vs 22-Gauge EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis (GUESS)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04770948
• Other study ID #: SPL822
• Status: Completed
• Phase: N/A
• Start date: March 1, 2021
• Est. completion date: September 30, 2023

Study information

• Verified date: November 2023
• Source: Postgraduate Institute of Medical Education and Research
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Sarcoidosis is an idiopathic disorder characterized by granulomatous inflammation involving various organ systems. The lung and mediastinal lymph nodes are the most commonly involved structures in sarcoidosis. In the presence of intrathoracic lymph nodes, transbronchial needle aspiration (TBNA) is a useful diagnostic modality, which is now guided using endobronchial ultrasound (EBUS).

We hypothesize that the 19-gauge EBUS-TBNA needle will have a higher yield as compared to the conventional 22-gauge EBUS-TBNA needle in intrathoracic lymphadenopathy due to sarcoidosis. In this study, we plan to evaluate the yield and safety of the 19-gauge needle vs. the conventional 22-gauge EBUS-TBNA needle in patients with sarcoidosis.

Description:

Sarcoidosis is an idiopathic disorder characterized by granulomatous inflammation involving various organ systems. The disease is diagnosed based on a suggestive clinicoradiological picture and the presence of non-caseating granulomas in the involved organ, after excluding known causes of granulomatous inflammation. The lung and mediastinal lymph nodes are the most commonly involved structures in sarcoidosis. Various bronchoscopic techniques such as endobronchial biopsy (EBB), transbronchial biopsy (TBLB) and transbronchial needle aspiration (TBNA) are commonly used for acquiring tissue samples.

In the presence of intrathoracic lymph nodes, TBNA is a useful diagnostic modality, especially when combined with endobronchial and transbronchial biopsies. At most centers, TBNA is now guided using endobronchial ultrasound (EBUS). The technique is minimally invasive and also offers the advantage of a selection of the appropriate node for sampling based on the ultrasonographic characteristics. Several studies have demonstrated the superiority of EBUS-TBNA over conventional TBNA (TBNA performed without real-time guidance).

Several technical aspects of EBUS-TBNA have been studied to optimize the yield including the number of aspirations or passes required per lymph node station, needle gauge (21 vs. 22 gauge), suction pressure, the distance travelled by the needle within the lymph node, the number of needle agitations required during a pass, and others.

The novel 19-G Vizishot FLEX EBUS needle (Olympus) is composed of a more flexible material (nitinol) than the 22-G EBUS needle. This allows it to have a larger inner diameter with the same outer diameter as a 22-G EBUS needle. Recent studies have shown that the 19-G needle is safe and has a comparable yield to smaller bore needles. In case of suspected lymphadenopathy due to malignant disorders, aspiration using smaller gauge needles may yield sufficient material for diagnosis. However, in sarcoidosis, larger nodal tissue obtained with a thicker bore needle, the 19-gauge needle, may potentially increase the identification of granulomas. We hypothesize that the 19-gauge EBUS-TBNA needle will have a higher yield as compared to the conventional 22-gauge EBUS-TBNA needle in intrathoracic lymphadenopathy due to sarcoidosis. In this study, we plan to evaluate the yield and safety of the 19-gauge needle vs. the conventional 22-gauge EBUS-TBNA needle in patients with sarcoidosis.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: September 30, 2023
• Est. primary completion date: February 28, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria: All the following

• Age at least 18 years

• Clinicoradiological suspicion of sarcoidosis where EBUS-TBNA is being planned

• Enlarged bilateral hilar and/or mediastinal lymph nodes >10 mm (any axis) on computed tomography of the chest

• Ability to provide informed consent to participate in the study.

Exclusion Criteria: Patients with any of the following will be excluded

• Asymmetric lymph nodes

• Lymph nodes with significant hypodense areas suggestive of necrosis

• Tuberculin skin test >10 mm

• Hypoxemia (SpO2 <92% on FiO2 of 0.3)

• Treatment with systemic glucocorticoids for >2 weeks in the preceding three months

• Diagnosis of sarcoidosis possible with another minimally invasive technique such as skin biopsy or peripheral lymph node biopsy

• Failure to provide informed consent.

Related Conditions & MeSH terms

• Sarcoidosis

Intervention

Device:
• 19 gauge needle
EBUS-TBNA performed using 19G needle
• 22 gauge needle
EBUS-TBNA performed using 22G needle

Locations

Country	Name	City	State
India	PGIMER	Chandigarh

Sponsors (10)

Lead Sponsor

Collaborator

Postgraduate Institute of Medical Education and Research

All India Institute of Medical Sciences, Bhopal, All India Institute of Medical Sciences, New Delhi, Apollo Hospitals Enterprise Limited, Asian Institute of Gastroenterology, Hyderabad, City Clinic and Bhailal Amin General Hospital, Vadodara, Institute of Pulmonology, Medical Research, and Development, Mumbai, Jaipur Golden Hospital, New Delhi, Rajiv Gandhi Cancer Institute & Research Center, India, Yashoda Hospitals, Hyderabad

Country where clinical trial is conducted

India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Diagnostic yield of EBUS-TBNA samples	Specimen showing epithelioid cell granulomas or collection of epithelioid cells with a giant cell (or asteroid body or Schaumann body).	6 months
Secondary	Adequacy of EBUS-TBNA samples	Specimen shows a preponderance of lymphocytes or is diagnostic	7 days
Secondary	Complication rate	Complication associated with EBUS-TBNA procedure	7 days
Secondary	Cough visual analog scale (VAS)	Operator-rated visual analog scale (VAS) score for the intensity of subject's cough	1 day
Secondary	Operator VAS	VAS score for ease of performance of the needle puncture and aspiration rated by the operator	1 day