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Assessment of pulmonary function of target area in lung cancer patients undergoing pulmonary reoperation and prediction of postoperative pulmonary function

Assessment of pulmonary function of target area in lung cancer patients undergoing pulmonary reoperation and prediction of postoperative pulmonary function

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200061325
Enrollment
Unknown
Registered
2022-06-21
Start date
2022-06-06
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

lung cancer

Interventions

1: Perfusion Scintigraphy
2:Three-dimensional reconstruction of chest CT

Sponsors

Department of Thoracic Surgery, the Fifth Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign informed consent; 2. Lung cancer patients who underwent pulmonary resection again after MDT discussion and evaluation in our hospital; 3. Older than 18 years of age, equal to or less than 75 years of age.

Exclusion criteria

Exclusion criteria: 1. Patients with pulmonary embolism and bronchial asthma; 2. Pregnant or lactating women; A history of severe allergy or allergy to contrast agent (99MTC-MAA); 3. Any unstable systemic disease, including active infection, left and right shunt congenital heart disease, pulmonary arteriovenous fistula and severe lung damage, uncontrolled hypertension, unstable angina, myocardial infarction (6 months), heart function failure (cardiac function grade III or above), severe arrhythmia, severe liver and kidney disease; 4. Severe blood system and related diseases, such as severe granulocytopenia and platelets Hypoxia and aplastic anemia; 5. Neurological and related diseases; 6. Participants in drug clinical trials within the last 3 months; 7. MDT discussion determined that the patient was not suitable for inclusion. These include advanced tumors, atelectasis, and encapsulated pleural effusion.

Design outcomes

Primary

MeasureTime frame
postoperative FEV1;Prediction of Postoperative Forced Expiratory Volume in 1 Sec (FEV1) by Perfusion Scintigraphy;Prediction of Postoperative Forced Expiratory Volume in 1 Sec (FEV1) by Three-dimensional reconstruction of chest CT;

Countries

China

Contacts

Public ContactQingdong Cao

the Fifth Affiliated Hospital of Sun Yat-sen University

Cqd8866@163.com+86 13680356988

Outcome results

None listed

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