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Clinical Trial

18G Ultrafine Cryoablation Needle for Coaxial Biopsy and Cryoablation of Pulmonary Nodules

NCT: NCT07806981 · NOT_YET_RECRUITING

NCT IDNCT07806981
StatusNOT_YET_RECRUITING
Start Date2026-09-01
Completion2030-04-01
SponsorShanghai Chest Hospital (OTHER)
First posted
Last updated

Brief Summary

This prospective, single-center clinical study will evaluate whether an 18-gauge ultrafine cryoablation needle can be used feasibly and safely during CT-guided coaxial transthoracic biopsy of pulmonary nodules. Approximately 30 adults with pulmonary nodules highly suspected of malignancy who are unsuitable for or decline surgery or radiotherapy will undergo biopsy and cryoablation during the same procedure. The study will assess technical success, biopsy diagnostic performance, imaging-based local control, and device- or procedure-related adverse events. Participants will be followed for up to 36 months. The study hypothesis is that the same-tract procedure is technically feasible and provides acceptable safety and local disease control.

Frequently Asked Questions

What is 18G Ultrafine Cryoablation Needle for Coaxial Biopsy and Cryoablation of Pulmonary Nodules?

18G Ultrafine Cryoablation Needle for Coaxial Biopsy and Cryoablation of Pulmonary Nodules is a clinical trial registered under NCT07806981. Current status: NOT_YET_RECRUITING.

What is the status of NCT07806981?

The current status of NCT07806981 (18G Ultrafine Cryoablation Needle for Coaxial Biopsy and Cryoablation of Pulmonary Nodules) is: NOT_YET_RECRUITING.

When did 18G Ultrafine Cryoablation Needle for Coaxial Biopsy and Cryoablation of Pulmonary Nodules start?

18G Ultrafine Cryoablation Needle for Coaxial Biopsy and Cryoablation of Pulmonary Nodules started on 2026-09-01.

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Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.