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Respiratory Acoustic Features in Association With Postoperative Pulmonary Complications Following Lung Surgery: A Single-Center Prospective Exploratory Study

Respiratory Acoustic Features in Association With Postoperative Pulmonary Complications Following Lung Surgery: A Single-Center Prospective Exploratory Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128672
Enrollment
Unknown
Registered
2026-07-23
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Lung cancer

Interventions

Trial group:None

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age = 18 years; 2.Scheduled to undergo segmentectomy, lobectomy, or extended lobectomy; 3.Possesses basic communication skills, is able to understand the study protocol, and can comply with study requirements; 4.Is able to provide respiratory sound data at the time points specified by the study and, in the investigator’s judgment, can complete the necessary examinations and follow-up visits; 5.Voluntarily participates in this study and has signed a written informed consent form;

Exclusion criteria

Exclusion criteria: 1.Severe respiratory failure prior to the procedure, rendering the subject unable to cooperate with study assessments; 2.Long-term mechanical ventilation or tracheostomy; 3.Severe heart failure or other critical conditions that may significantly affect respiratory status and interfere with study evaluation; 4.Obvious skin lesions, infections, allergic rashes, or other conditions on the chest wall that make it unsuitable for device application; 5.Severe cognitive impairment, psychiatric disorders, or other conditions that prevent effective cooperation with the investigator; 6.Concurrent participation in other interventional clinical trials that may influence the interpretation of this study’s results; 7.Other circumstances deemed unsuitable for inclusion in this study by the investigator;

Design outcomes

Primary

MeasureTime frame
Postoperative complications;

Secondary

MeasureTime frame
System Data Collection Success Rate;Compliance score for wearing the device;

Countries

China

Contacts

Public ContactFeng Yao

Shanghai Chest Hospital

yaofeng6796678@126.com+86 21 2220 0000

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026