Skip to content

Diagnosis and treatment of early ground glass opacity in elderly patients

Diagnosis and treatment of early ground glass opacity in elderly patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037680
Enrollment
Unknown
Registered
2020-08-30
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

ground glass opacity

Interventions

Sponsors

Huadong Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) In patients with early ground-glass pulmonary nodules, the size of the nodules <= 19mm; (2) Elderly aged 70 or above; (3) The main organs function well and the blood clotting function is normal; (4) Before the subjects were enrolled, they signed informed consent to participate in the study and abide by the study procedures.

Exclusion criteria

Exclusion criteria: Patients with previous cancers, pneumonectomy for other reasons, patients with atelectasis, pleural effusion, multiple adenocarcinoma, preoperative radiotherapy and chemotherapy, etc. Specific standard is as follows: (1) can't control the systemic hemorrhagic diseases, serious high blood coagulation state, blood coagulation function disorder or subjects are using drugs affect the function of blood coagulation; (2) serious complications, such as heart function class III and IV (NYHA standard New York heart association), the occurrence of myocardial infarction within six months or more than 3 (including 3) angina pectoris, brain trauma, brain parasitic diseases, apoplexy, hepatic encephalopathy, autoimmune hepatitis, cirrhosis of the liver decompensation period patients with hepatic insufficiency, renal insufficiency; (3) Previous history of other malignant tumors, except cured basal cell carcinoma or squamous cell carcinoma of the skin and carcinoma in situ of the cervix; (4) The accompanying diseases (including but not limited to hypertension, severe diabetes, active infection, thyroid disease, etc.) that, according to the judgment of the researcher, seriously endanger the safety of the patient or affect the completion of the study; (5) Any mental or cognitive impairment, emotional instability, which may limit their understanding of informed consent, implementation, and compliance with the study; (6) Other conditions in which the researcher considers him/her unfit to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
1 year disease-free survival time;2 years disease-free survival time;quality of life;Major complications following RFA or surgical excision;

Countries

China

Contacts

Public ContactShen Xiaoyong

Huadong Hospital affiliated to Fudan University

hanson_shen@aliyun.com+86 13061609292

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026