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RECRUITING NA

Diagnostic Yield of Intranodal Forceps Biopsies in Mediastinal Adenopathy

NCT05374447 · View on ClinicalTrials.gov ↗

Study Summary

The investigators will compare endobronchial ultrasound transbronchial needle aspiration (EBUS-TBNA) with intranodal forceps biopsy (EBUS-IFB) as it relates to the rate of diagnosis of suspected sarcoidosis.

Interventions

  • PROCEDURE Endobronchial Ultrasound-Guided Intranodal Forceps Biopsy

Study Locations (1)

District of Columbia

  • The George Washington University Hospital — Washington D.C.

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2022-06-10
Est. Completion 2026-03-01
Phase NA

Sponsor

George Washington University

134 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05374447

The ClinicalTrials.gov registry entry for NCT05374447 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 55 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is George Washington University, which has 134 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Sarcoidosis, Pulmonary appearing as the primary indexed condition, and to 1 intervention — of which Endobronchial Ultrasound-Guided Intranodal Forceps Biopsy is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05374447 reports 1 study location spanning 1 distinct geographic area — top geographies include District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05374447 about?

NCT05374447 is a clinical study titled "Diagnostic Yield of Intranodal Forceps Biopsies in Mediastinal Adenopathy". The investigators will compare endobronchial ultrasound transbronchial needle aspiration (EBUS-TBNA) with intranodal forceps biopsy (EBUS-IFB) as it relates to the rate of diagnosis of suspected sarcoidosis.

What is the current status of trial NCT05374447?

This trial is currently recruiting. It is a NA study. The enrollment target is 55 participants. The study started on 2022-06-10. Estimated completion is 2026-03-01.

What conditions does trial NCT05374447 study?

This clinical trial studies the following conditions: Sarcoidosis, Pulmonary, Mediastinal Lymphadenopathy, Mediastinal Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05374447?

The interventions under investigation include: Endobronchial Ultrasound-Guided Intranodal Forceps Biopsy (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05374447?

This trial is sponsored by George Washington University, which has 134 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05374447 being conducted?

This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial