Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06593106

Cryodevitalization for the Treatment of Early Stage Lung Cancer, CRYSTAL Trial

Led by Vanderbilt-Ingram Cancer Center · Updated on 2026-02-02

30

Participants Needed

1

Research Sites

100 weeks

Total Duration

On this page

Sponsors

V

Vanderbilt-Ingram Cancer Center

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This clinical trial studies side effects and best treatment time of cryodevitalization in treating patients with early stage (stage I or stage II) lung cancer. Cryodevitalization is a type of cryosurgery that uses a flexible probe (cryoprobe) to kill tumor cells by freezing them. It is delivered at the time of standard diagnostic robotic bronchoscopy. Using cryodevitalization may be safe, tolerable and/or effective in treating patients with early stage lung cancer.

CONDITIONS

Official Title

Cryodevitalization for the Treatment of Early Stage Lung Cancer, CRYSTAL Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with a single lung nodule 3 centimeters or smaller confirmed as malignant or oligometastatic disease during biopsy
  • Nodules located in the outer two-thirds of the lung, more than 10 mm from the pleura and large blood vessels or mediastinal structures
  • Patients eligible for surgical tumor removal based on imaging, lung function (FEV1 > 40%), and medical evaluation
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Lung nodules located within the central zone or less than 10 mm from the pleura
  • Expected survival less than 6 months
  • Presence of endobronchial lesions suspicious for cancer seen on initial bronchoscopy
  • Uncorrectable bleeding disorders (platelet count < 100 x 10^9/L or INR > 1.5)
  • Known pulmonary hypertension with pulmonary artery systolic pressure over 50 mmHg
  • Current use of anticoagulants, clopidogrel, or platelet inhibitors
  • Medical conditions making surgery high-risk
  • Pregnant women
  • Unable to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Vanderbilt University/Ingram Cancer Center

Nashville, Tennessee, United States, 37203

Actively Recruiting

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Research Team

V

Vanderbilt-Ingram Services for Timely Access

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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