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Study of Ablation for the Pulmonary Focal Pure Ground Glass Opacity (pGGO)

A Prospective Study of Ablation of Pulmonary Focal Pure Ground Glass Opacity

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01429649
Acronym
pGGO
Enrollment
100
Registered
2011-09-07
Start date
2011-09-30
Completion date
2014-12-31
Last updated
2011-09-07

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

Conditions

Pulmonary Lesions

Keywords

pure pulmonary ground glass opacity

Brief summary

With the advent of CT screening for lung cancer, there is an increase in the detection of pulmonary lesions with focal pure ground-glass opacity (pGGO). The pure Ground-glass opacities can be caused by normal expiration, partial filling of air spaces, partial collapse of alveoli, interstitial thickening, inflammation, oedema, fibrosis, and lepidic proliferation of neoplasm. Precise details of the natural history of focal pure GGO are still largely unclear. A number of differential diagnoses are possible, including inflammatory disease, focal scar, atypical adenomatous hyperplasia (AAH), and adenocarcinoma in situ. Some of pGGOs remained stable over a considerable time. A long doubling time for pGGOs is already known. Therefore, the strategy of treatment for focal pure GGO lesions is still undecided. The major issue is whether or not the doctors should treat these patients at all or wait until the first sign of a solid lesion developes which may take many years. The purpose of this study is to determine if the ablation therapy is safe and effective for the pulmonary pGGO.

Interventions

PROCEDUREcryotherapy or radiofrequency ablation

Cryoablation or Radiofrequency ablation is performed under CT image guidance.

Sponsors

Dongfang Hospital Beijing University of Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* The lesion(s) treated with ablation must be =\< 2.0 cm in greatest dimension * All patients are required to have been evaluated in a multi-disciplinary tumor conference to ensure that the lesion is suitable for Image-guided percutaneous ablation * Platelet count ≥ 100 x 109/L * International normalized ratio (INR) \< 1.5 * Absolute neutrophil count (ANC) ≥ 1.5 x 109/L * A signed study specific consent form is required

Exclusion criteria

* Direct evidence of regional or distant metastases,or synchronous primary or prior malignancy in the past 5 years * Unable to lie flat or has respiratory distress at rest * Uncontrolled coagulopathy or bleeding disorders * Evidence of active systemic, pulmonary, or pericardial infection * Women who are pregnant or breastfeeding * Patients with poor pulmonary function

Design outcomes

Primary

MeasureTime frameDescription
The changing of the lesion3 yearsTo determine the efficacy rate of CT image guided ablation for pulmonary focal pGGO. To determine the feasibility and safety of CT image guided ablation in patients with pulmonary pGGO.

Secondary

MeasureTime frameDescription
The side effect of the therapy.3 yearsIntra and post-operative complications rates. Quality-of-life assessment

Countries

China

Contacts

Primary ContactWeisheng Chen, MD
weishengmd@hotmail.com+8618960826090

Outcome results

None listed

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