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A prospective case-control study to improve the diagnostic yield of sarcoidosis with a new 19g TBNA needle

A prospective case-control study to improve the diagnostic yield of sarcoidosis with a new 19g TBNA needle

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073994
Enrollment
Unknown
Registered
2023-07-26
Start date
2023-07-26
Completion date
Unknown
Last updated
2023-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sarcoidosis

Interventions

Gold Standard:Combining the pathological results of biopsy and the therapeutic effect after six months of treatment
Index test:pathological test from a specimen obtained by a 19G EBUS-TBNA needle
pathological test from a specimen obtained by a 22G EBUS-TBNA needle

Sponsors

Peking Union Medical Collage Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age at least 18 years 2. Clinical suspicion of sarcoidosis where EBUS-TBNA is being planned 3. Enlarged bilateral hilar and/or mediastinal lymph nodes >10 mm (any axis) on computed tomography of the chest 4. Ability to provide informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Asymmetric lymph nodes 2. Treatment with systemic glucocorticoids for >2 weeks in the preceding three months 3. Diagnosis of sarcoidosis possible with another minimally invasive technique such as skin biopsy or peripheral lymph node biopsy 4. Other test results verify the diagnosis of tuberculosis 5. Failure to provide informed consent.

Design outcomes

Primary

MeasureTime frame
diagnostic yield of sarcoidosis with a new 19g TBNA needle;

Secondary

MeasureTime frame
diagnostic yield of sarcoidosis with a new 19g TBNA needle together with TBLB;diagnostic yield of sarcoidosis with a new 19g TBNA needle together with EBB;

Countries

China

Contacts

Public ContactShao chi

Peking Union Medical Collage Hospital

shaochi@live.com+86 138 1021 9574

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026