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Analysis of the optimal suction pressure at the time of the Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA)

Analysis of the optimal suction pressure at the time of the Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) - Analysis of the optimal suction pressure at the time of the Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000039765
Enrollment
85
Registered
2020-03-11
Start date
2020-03-11
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

human mediastinal/hilar lymph node lesions

Interventions

None listed

Sponsors

Fujita Health University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Examination with bronchoscope is necessary for the diagnosis of the pulmonary lesion regardless of the participation of this study, is the case using a supersonic wave device (EBUS) and the guide sheath (GS) at the time of inspection. 2.The case that a document agreement by the free will of the person was provided on enough understanding after having received enough explanation on participating of this study 3.It is a case younger than 90 years 20 years old or older at the time of the agreement acquisition 4.Longer axis 2cm or less of the target lesion in the chest CT 5.The case that thin slice CT less than slice thickness 2mm is photographed in examination with bronchoscope precordial region CT

Exclusion criteria

Exclusion criteria: 1.A case with pneumothorax that is clear before examination. 2.The case that merges respiratory failure (PaO2 <60torr) 3.It is a case of blood pressure vital measurement just before the examination with bronchoscope start for the shrinkage period 4.In addition, the case that a manager for study, a study partaker judged to be inappropriate.

Design outcomes

Primary

MeasureTime frame
Diagnostic tissue (the area of a pathological sample useful in disease diagnosis; a parameter of sample quantity) and damaged area in tissue (percentage of damaged tissue area in the total tissue area; a parameter of sample quality) were compared as primary endpoints between the two groups.

Countries

Japan

Contacts

Public ContactTomoyuki Minezawa

Fujita Health University School of Medicine Department of Respiratory Medicine

minezawa@fujita-hu.ac.jp0562-93-9241

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026