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Transthoracic ultrasonography in the diagnosis of pleural adhesion before video-assisted thoracic surgery: a multicenter diagnostic study

Transthoracic ultrasonography in the diagnosis of pleural adhesion before video-assisted thoracic surgery: a multicenter diagnostic study

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100044969
Enrollment
Unknown
Registered
2021-04-03
Start date
2021-04-12
Completion date
Unknown
Last updated
2021-11-02

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

Conditions

Pleural adhesion

Interventions

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diagnosis&#32
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adhesion
Gold Standard:During the surgery, the first thoracoscopic lens was placed into the chest to record the location and extent of the pleural adhesions under direct vision.In this study, pleural adhesion
in&#32

Sponsors

Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective VATS chest surgery; 2. Patients with a history of congestive heart failure, tumor, ipsilateral thoracic surgery, ipsilateral epigastric surgery, chest trauma, chemotherapy, chest radiation therapy, immunotherapy, pulmonary infection (tuberculosis, pneumonia, and/or bronchiectasis), COPD, pulmonary embolism, and/or pleural fixation; 3. At least 18 years old; 4. No serious visual and hearing impairments, able to read text; 5. Patients participated voluntarily and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who cannot cooperate with follow-up or have poor compliance; 2. The general condition of the patient is poor, with a history of severe cardiovascular system, respiratory system, liver and kidney system, central nervous system and other diseases, and it may be difficult for the patient to survive for more than 3 months; 3. pregnant women; 4. Acute myocardial infarction, cardiac arrest or shock during surgery or hospitalization; 5. The investigator believes that there are any factors that may affect the participants' participation in the study or the evaluation of the results.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;

Countries

China

Contacts

Public ContactWei Xing

The Department of Anesthesiology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine

xingwei@sysucc.org.cn+86 20 87343060

Outcome results

None listed

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