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NCT04529603

The Efficacy of Intraoperative Pulmonary Nodules Localization Guided by Virtual Reality Technology

Withdrawn NA Last updated 2 September 2021
What this trial tests

NA trial testing LungBrella marker implantation and VATS partial lobe resection in Lung Neoplasm. Withdrawn.

Timeline
1 December 2020
Primary endpoint
1 August 2022
1 October 2022

Quick facts

Lead sponsorRuijin Hospital
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date1 December 2020
Primary completion1 August 2022
Estimated completion1 October 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Ruijin Hospital

Who can join

Adults 18 to 70, any sex, with Lung Neoplasm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

As the detection of small pulmonary nodules continuously grows, the intraoperative localization of small pulmonary nodules is in great demand. The intraoperative localization nowadays is usually done under local anesthesia before surgery. There is a certain rate of failure and complication. The result of our early animal experiments show that the pulmonary surgery marker system can deliver the intraoperative localization safely and precisely under anesthesia, and the average distance between the localization and the simulated lesion is less than 5mm during surgery. Therefore, the safety and feasibility of the system require further evaluation in patients

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of LungBrella marker implantation and VATS partial lobe resection

Trials testing the same drug.

Other recruiting trials for Lung Neoplasm

Currently open trials in the same condition.

Other Ruijin Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04529603.

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