EBUS-GS-TBLB With or Without Fluoroscopy for the Diagnosis of PPLs

Sponsor
Shanghai Chest Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01895166
Collaborator
Fukushima Medical University (Other)
100
1
2
11
9.1

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the efficacy and safety of endobronchial ultrasound-guide sheath(EBUS-GS) for the diagnosis of peripheral pulmonary lesions (PPLs) without radiographic fluoroscopy.

Condition or Disease Intervention/Treatment Phase
  • Procedure: EBUS-GS
  • Procedure: X-ray
N/A

Detailed Description

The investigators evaluated the efficacy and safety of transbronchial biopsy (TBB) and bronchial brushing by endobronchial ultrasonography (EBUS) with a guide sheath (GS) as a guide for diagnosing peripheral pulmonary lesions (PPLs) without radiographic fluoroscopy.The study is designed as a two-center prospective randomized controlled trial. The participating centers are Department of pulmonary medicine and endoscope center, Shanghai chest Hospital affiliated to Shanghai JiaoTong University School, China. Department of pulmonary medicine, Fukushima Medical University, Japan.Patients are divided into two groups, EBUS-GS-X-ray group and EBUS-GS group.Each subject will be randomized to each group.The study is expected to enroll 100 patients at 2 centers (China:75, Fukushima:25).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Diagnostic Value of Endobronchial Ultrasound(EBUS) With a Guide Sheath(GS) for Peripheral Pulmonary Lesions(PPLs) Without Fluoroscopy: a Randomized Controlled Trial
Study Start Date :
Jul 1, 2013
Anticipated Primary Completion Date :
Jun 1, 2014
Anticipated Study Completion Date :
Jun 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: EBUS-GS group

The EBUS probe and GS are confirmed to reach the lesion by EBUS images alone, cytologic and pathologic specimens are obtained without fluoroscopic guidance.

Procedure: EBUS-GS
EBUS is performed using an endoscope ultrasound system , which is equipped with a 20-MHz mechanical radial-type probe (UM-S20-17S;Olympus) with an external diameter of 1.4 mm and a GS (K-201; Olympus).

Active Comparator: EBUS-GS-X-ray group

The EBUS probe and GS are confirmed to reach the lesion by EBUS images and radiograph fluoroscopy, cytologic and pathologic specimens are obtained under fluoroscopic guidance.

Procedure: EBUS-GS
EBUS is performed using an endoscope ultrasound system , which is equipped with a 20-MHz mechanical radial-type probe (UM-S20-17S;Olympus) with an external diameter of 1.4 mm and a GS (K-201; Olympus).

Procedure: X-ray
The radiograph fluoroscopy are performed when the probe and GS are confirmed to reach the lesion by EBUS images ,cytologic and pathologic specimens are obtained under fluoroscopic guidance.

Outcome Measures

Primary Outcome Measures

  1. The difference of diagnostic value of EBUS-GS-TBLB with fluoroscopy as compared to EBUS-GS-TBLB alone [Up to half year]

    The diagnostic value mean sensitivity and specificity in two groups

Secondary Outcome Measures

  1. The difference of complications of EBUS-GS-TBLB with fluoroscopy as compared to EBUS-GS-TBLB alone [Up to half year]

    Complications mean a composite of operation-related serious adverse events (pneumothorax, bleeding, etc.) during and after the operation in two groups

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Individuals eligible for inclusion are patients that the CT scan appearance of the PPLs showed the longest diameter was more than 2 cm and solid lesions.
Exclusion Criteria:
  1. The lesion is close to the pleural membrane

  2. Refusal of participation

  3. Severe cardiopulmonary dysfunction and other indications that can't receive bronchoscopy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shanghai Chest Hospital Shanghai China 200030

Sponsors and Collaborators

  • Shanghai Chest Hospital
  • Fukushima Medical University

Investigators

  • Principal Investigator: Jiayuan Sun, MD, Shanghai Chest Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jiayuan Sun, Director, Endoscope Center, Shanghai Chest Hospital, Shanghai Chest Hospital
ClinicalTrials.gov Identifier:
NCT01895166
Other Study ID Numbers:
  • SHCHE201301
First Posted:
Jul 10, 2013
Last Update Posted:
Jul 31, 2013
Last Verified:
Jul 1, 2013
Keywords provided by Jiayuan Sun, Director, Endoscope Center, Shanghai Chest Hospital, Shanghai Chest Hospital

Study Results

No Results Posted as of Jul 31, 2013