Application of Intraoperative Indocyanine Green Inhalation

Intraoperative Detection of Pleural Defect with Indocyanine Green Inhalation

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300067603

Enrollment

Unknown

Registered

2023-01-13

Start date

2023-01-15

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

Lung Nodules

Interventions

experimental group:inhalation of indocyanine green

control group:none

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients intended to underwent VATS anatomical lung resection; 2.Age between 18-80; 3.Patients himself voluntarily signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients who are allergic to ICG; 2.Patients with asthma; 3.Patients with the history of thoracic surgery; 4.Patients with infectious disease (Hepatitis B, Hepatitis C, syphilis, AIDS and so on); 5.Patients deemed unsuitable by the investigator.

Design outcomes

Primary

Measure	Time frame
Postoperative air leak rate;	—

Secondary

Measure	Time frame
Detection time;Chest tube duration;Postoperative prolonged air leak;	—

Countries

China

Contacts

Public ContactZhou Jian

Peking University People's Hospital

zhoujian@bjmu.edu.cn+86 10 88326655

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026