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Three-Dimensional printing template for intraoperative localization of pulmonary nodules in the pleural cavity: A pilot study

Three-Dimensional printing template for intraoperative localization of pulmonary nodules in the pleural cavity: A pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049139
Enrollment
Unknown
Registered
2021-07-23
Start date
2021-07-31
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Lung Cancer

Interventions

Experimental group:Intrathoracic localization of pulmonary nodules

Sponsors

The First Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 80 years; 2. Nodules around the lungs with clear chest CT (the nodules are located in 1/3 of the lung field); 3. Measured under the lung window of chest CT, the maximum diameter of the target nodule is less than or equal to 20mm; 4. The minimum distance from the edge of the completely solid nodular lesion to the pleura is >=10mm; 5. Assessed by the attending physician, the patient has indications for wedge resection of pulmonary nodules, and is planned to undergo traditional CT-guided preoperative positioning; 6. Patients participate voluntarily and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients without preoperative positioning under traditional CT guidance due to any reason; 2. The patient has complications related to pneumothorax and hemothorax during preoperative puncture, and the clinician judges that the patient is no longer suitable for intraoperative positioning and needs to withdraw from the trial; 3. Patients with extensive adhesions in the thoracic cavity due to previous thoracic surgery or chest diseases are not suitable for intraoperative positioning; 4. The patient requests to withdraw from the trial.

Design outcomes

Primary

MeasureTime frame
Distance between lung surface design and actual anchor point;

Secondary

MeasureTime frame
Distance between stain marker and lesion center;Design location distance between lesion and lung surface;time of duration;the number of operations;

Countries

China

Contacts

Public ContactMa Minjie

The First Hospital of Lanzhou University

th1251264818@163.com+86 16628768769

Outcome results

None listed

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