Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05283564

Study to Evaluate Percussive Ventilation Breathhold to Improve Lung Stereotactic Ablative Radiotherapy

Led by Stanford University · Updated on 2025-07-15

20

Participants Needed

1

Research Sites

200 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this research is to evaluate and determine the rate of successful administration of Percussive ventilation breathhold (PVB) to allow for more accurate radiotherapy for lung tumors.

CONDITIONS

Official Title

Study to Evaluate Percussive Ventilation Breathhold to Improve Lung Stereotactic Ablative Radiotherapy

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy volunteers aged 18 or older
  • Ability to understand and willingness to sign the written informed consent
  • Patients diagnosed with primary lung cancer or lung metastases of any origin
  • Patients eligible for standard lung SABR treatment
  • Patients aged 18 or older of any gender
  • Patients with ECOG Performance Status 0-2 or select patients with Performance Status 3 deemed suitable
  • Ability to understand and willingness to sign the written informed consent
Not Eligible

You will not qualify if you...

  • Pregnant individuals or those with recent pregnancy (last menstrual period within the previous 12 months) among healthy volunteers
  • Patients deemed ineligible for standard lung SABR treatment (e.g., due to excessive tumor size, pregnancy, breastfeeding, or severe pulmonary fibrosis)
  • Patients with newly developed pneumothorax
  • Patients with critical acute illness preventing SABR (e.g., active pulmonary embolism or infection requiring inpatient care)
  • Patients with ECOG Performance Status 4

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

Stanford Cancer Institute

Palo Alto, California, United States, 94305

Actively Recruiting

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Research Team

K

Kelly Huang

CONTACT

A

Anoushka Kathiravan

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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