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Clinical comparison of localization of pulmonary nodules by 3D precise localization based on anatomical markers and CT guided hookwire localization

Clinical comparison of localization of pulmonary nodules by 3D precise localization based on anatomical markers and CT guided hookwire localization

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031740
Enrollment
Unknown
Registered
2020-04-08
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-04-13

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

Conditions

Lung nodules

Interventions

Group 1:3D accurate localization of pulmonary nodules based on anatomical markers
Group 2:Localization of pulmonary nodules by preoperative CT guided percutaneous hookwire

Sponsors

Shenzhen Hospital of the University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Before any evaluation, the patient or his legal representative must sign the informed consent; 2. Patients aged 18 to 80 years; 3. Patients with normal civil capacity; 4. Patients who can sign informed consent independently; 5. The patients with SPN were confirmed by CT examination. On CT, SPN showed lung nodule lesions with clear boundary, diameter less than or equal to 3cm, surrounded by air containing lung tissue; 6. Patients with tolerance of operation and no contraindication of operation proved by the examination of organ function before operation; 7. Patients without coagulation dysfunction.

Exclusion criteria

Exclusion criteria: 1. Patients who do not agree to participate in the study program; 2. Patients who do not meet the clinical diagnosis of SPN; 3. The patients who underwent reoperation; 4. Patients with resection of other organs; 5. Patients who are converted to thoracotomy due to adhesion or intraoperative bleeding; 6. Patients with poor cardiopulmonary function who cannot tolerate general anesthesia.

Design outcomes

Primary

MeasureTime frame
The accurate rate of localization;

Secondary

MeasureTime frame
Time required for operation of two positioning methods;????? Total operation time;Location related complications;

Countries

China

Contacts

Public ContactDazhi Pang

Shenzhen Hospital of the University of Hong Kong

pangdz@hku-szh.org+86 13632998642

Outcome results

None listed

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