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Spots Global Cancer Trial Database for Vibration Response Imaging (VRI) in Patients Who Are Potential Candidates for Surgical Resection

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Trial Identification

Brief Title: Vibration Response Imaging (VRI) in Patients Who Are Potential Candidates for Surgical Resection

Official Title: Vibration Response Imaging (VRI) in Patients Who Are Potential Candidates for Surgical Resection

Study ID: NCT00966511

Conditions

Lung Cancer

Study Description

Brief Summary: The primary purpose of the study is to investigate the use of VRI to guide the selection of patients for lung surgery. Perfusion scintigraphy is the current method to assess the fractional contribution of lung function of the remaining lung. The hypothesis is that VRI can determine quantitative postoperative lung function equally accurately as a quantitative perfusion scan.

Detailed Description: Primarily, VRI will be compared to perfusion (Q) scan by predicted post-operative (ppo) FEV1 and DLCO as predicted by VRI versus as predicted by Q scan. Secondary, the ppo as predicted by each test will be compared with the actual FEV1 and DLCO at 3 months post-operative; If these two methods provide similar results, VRI will be deemed an acceptable alternative to Q scan for determining patient selection for lung resection. Finally, the patient outcomes (30 day mortality and pulmonary complications) for those patients falling within guideline parameters using the VRI measurement will be analyzed to see if using VRI in clinical practice would indeed allow prediction of satisfactory results (similar to literature benchmarks).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Yale University School of Medicine, New Haven, Connecticut, United States

Emory University, Atlanta, Georgia, United States

Boston Medical Center, Boston University, Boston, Massachusetts, United States

Mt. Sinai School of Medicine, New York, New York, United States

New York-Presbyterian Hospital/Columbia University Medical Center, New York, New York, United States

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Frank C Detterbeck, MD

Affiliation: Yale University Medical School

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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