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Intraoperative Ultrasonographic Localization of Pulmonary Nodules in VATS

Intraoperative Ultrasonographic Localization of Pulmonary Nodules in Video-assisted Thoracoscopic Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03599505
Enrollment
200
Registered
2018-07-26
Start date
2018-07-31
Completion date
2019-12-31
Last updated
2018-07-26

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

Conditions

Ultrasonography

Keywords

intraoperative ultrasonographic localization, pulmonary nodules, video-assisted thoracoscopic surgery

Brief summary

This study is conducted to explore the feasibility and value of Intraoperative ultrasonographic localization of pulmonary nodules in video-assisted thoracoscopic surgery (VATS).

Detailed description

The study is designed as a single center prospective trial. The participating center is Department of Ultrasound, Shanghai Chest Hospital, Shanghai Jiao Tong University, China. The study is expected to enroll 200 patients. The feasibility and value of Intraoperative ultrasonographic localization of pulmonary nodules in VATS will be explored. The accuracy rate of localization will be evaluated using gray scale mode and elastography mode. Intraoperative ultrasonographic localization will be performed using an ultrasound system (HI VISON Ascendus), which is equipped with a 5-10MHz mechanical probe (EUP-OL531).

Interventions

PROCEDURElocalization group

Intraoperative ultrasonographic localization will be performed using an ultrasound system (HI VISON Ascendus), which is equipped with a 5-10MHz mechanical probe (EUP-OL531). The accuracy rate of localization will be evaluated using gray scale mode and elastography mode.

Sponsors

Shanghai Chest Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients who are older than 18 year-old. 2. Chest CT shows pulmonary nodule suspected to be malignant that need to undergo VATS. 3. Patients who have good compliance and sign informed consent.

Exclusion criteria

1. Patient with severe asthma and pulmonary fibrosis. 2. Refusal of participation. 3. Severe cardiopulmonary dysfunction and other indications that can't receive VATS.

Design outcomes

Primary

MeasureTime frameDescription
The accuracy rate of localizationone yearThe accuracy rate of localization will be evaluated using gray scale mode and elastography mode using pathology as a reference.

Secondary

MeasureTime frameDescription
Correlation of lesion size and localizationone yearWhether lesion size affects localization will be explored in the study.
Correlation of distance between the lesion and pleura and localizationone yearWhether distance between the lesion and pleura affects localization will be explored.
Time of localizationone weekThe time of intraoperative ultrasonographic localization will be recorded.

Contacts

Primary ContactLei Wang, MD
13917985547@163.com86-021-22200000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026