Overview

Lipiodol Localization for Ground-glass-opacity Minimal Surgery

Status:
Completed
Trial end date:
2017-12-01
Target enrollment:
0
Participant gender:
All
Summary
The study object is to demonstrate the usefulness and safety of lipiodol localization technique for individuals undergoing ground-glass opacity (GGO) Video-assisted thoracic surgery (VATS) resection compared to hook wire localization technique. A total of 250 participants will be enrolled in a 1:1 fashion to Lipiodol or Hook-wire groups. If the aims of this study are achieved, the use of lipiodol localization technique will be widespread their application for localization of non-palpable pulmonary lesions that are indicated for VATS resection.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Severance Hospital
Collaborators:
Asan Medical Center
Chung-Ang University Hosptial, Chung-Ang University College of Medicine
Dankook University
Gangnam Severance Hospital
Korea University Anam Hospital
Pusan National University Hospital
Wonju Severance Christian Hospital
Treatments:
Ethiodized Oil
Criteria
Inclusion Criteria:

- Consenting adult patients ≥ 20 years of age

- Pulmonary lesion with a ground glass opacity(GGO)component of more than 50%

- Patient with lesion size less than 3cm

- Persistence or growth of the established lesion within a three month period

- Patient who are not contraindicated to surgery

- Patients who are willing to sign the informed consent form

Exclusion Criteria:

- Patients with solid pulmonary lesion

- Patients with multiple GGOs need multiple localization

- Patients who are contraindicated to surgery

- Patients who behave in an uncooperative manner

- Unwilling or unable to give informed consent

- Pregnant women