Single Pulmonary Nodule Investigation (SPUtNIk)
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|ClinicalTrials.gov Identifier: NCT02013063|
Recruitment Status : Recruiting
First Posted : December 17, 2013
Last Update Posted : October 18, 2016
A small proportion of patients with lung cancer present with a solitary pulmonary nodule (SPN). This is an important group of patients because if it is lung cancer, presentation as a SPN represents early disease, which following surgery has a high 5 year survival rate. However as not all SPNs are lung cancer it would be unethical to biopsy every case. Clinical guidelines recommend that SPNs should undergo an initial (FDG)-PET/CT scan, which may give more information about the SPN and may indicate if it is likely to be lung cancer. However in many cases it does not and current practice is to monitor the SPN with a series of CT scans over 2 years to look for changes or growth which may/ but not always indicate lung cancer. If no changes are observed over 2 years the SPN is considered not lung cancer. This is both expensive for the National Health Service (NHS) and worrying for the patient in terms of monitoring CT costs and delayed treatment due to length of time to diagnosis.
This study examines the diagnostic capacity of using a different CT scan. Dynamic Contrast Enhanced -CT(DCE-CT). DCE-CT and FDG-PET/CT scans give different information about the SPN and the investigators will look to see if information from either scan or combined information from both scans may be better in the diagnosis of early stage lung cancer. The investigators will also undertake a review of previous studies that have used these scans and use data from both the review and the trial to look at the cost effectiveness of using DCE-CT in the diagnosis of SPN.
The trial will recruit 375 people who have a SPN detected by a normal CT scan which requires a FDG-PET/CT scan. In addition they will receive a DCE-CT scan either on the same day or within three weeks of the FDG-PET/CT scan. This is the only extra procedure that will take place to normal NHS care, however we will collect clinical and outcome data over the next two years.
The study is coordinated by Southampton University clinical trials unit. Recruitment between January 2013 - April 2016, from up to 14 UK sites. Data analysis and conclusions are expected by the end of 2018.
The study is funded by the NIHR-HTA
|Condition or disease|
|Malignant Neoplasm of Lung|
Show Detailed Description
|Study Type :||Observational|
|Estimated Enrollment :||375 participants|
|Official Title:||Accuracy and Cost-Effectiveness of Dynamic Contrast Enhanced Computed Tomography in the Characterisation of Solitary Pulmonary Nodules|
|Study Start Date :||August 2012|
|Estimated Primary Completion Date :||October 2018|
|Estimated Study Completion Date :||October 2018|
- Effectiveness of DCE-CT scans and FDG-PET scans to diagnose early lung cancer in SPN [ Time Frame: 2 years ]Primary outcome measures will include diagnostic test characteristics (sensitivity, specificity, accuracy) for 18FDG-PET/CT and DCE-CT in relation to a subsequent clinical diagnosis of lung cancer.
- cost effectiveness of using DCE-CT scans in the diagnosis of early lung cancer in SPN [ Time Frame: 2 years ]The outcome measures used in the economic model will include accuracy, estimated life expectancy, and quality adjusted life years (QALYs). Costs will be estimated from an NHS perspective. Incremental cost-effectiveness ratios will compare management strategies with DCE-CT to strategies without DCE-CT.
- Effectiveness of DCE-CT scans combined with FDG-PET scans to diagnose early lung cancer in SPN [ Time Frame: 2 years ]Diagnostic test characteristics combined DCE-CT/18FDG-PET in relation to a subsequent clinical diagnosis of lung cancer.
- Effectiveness of using analysis of the CT image from the FDG-PET/CT in conjunction with data from the FDG incorporation to diagnose early lung cancer in SPN [ Time Frame: 2 years ]Diagnostic test characteristics for 18FDG-PET/CT with incorporation of CT appearances in relation to a subsequent clinical diagnosis of lung cancer.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02013063
|Contact: Jackie Madden, PhDemail@example.com|
|Contact: Louisa Littlefirstname.lastname@example.org|
|Southampton University Hospitals Nhs Trust||Recruiting|
|Southampton, Hampshire, United Kingdom, SO16 6YD|
|Principal Investigator: Anindo Dr Banerjee, PhD|
|Western Sussex Hospitals NHS Foundation Trust||Recruiting|
|Worthing, Sussex, United Kingdom, BN112DH|
|Contact: Nick Adams, MD FRCP|
|Aberdeen, United Kingdom, AB25 2ZN|
|Principal Investigator: Lesley Gomersall, MD|
|Brighton and Sussex University Hospitals Nhs Trust||Recruiting|
|Brighton, United Kingdom, BN2 5BE|
|Principal Investigator: Sabina Dr Dizdarevic, MD|
|Papworth Hospital Nhs Foundation Trust||Recruiting|
|Cambridge, United Kingdom, CB23 3RE|
|Principal Investigator: Nagmi Dr Qureshi, M.B.|
|NHS Greater Glasgow and Clyde||Recruiting|
|Glasgow, United Kingdom, G116NT|
|Principal Investigator: Sai Han, MBChB|
|Leeds Teaching Hospitals Nhs Trust||Recruiting|
|Leeds, United Kingdom, LS9 7TF|
|Principal Investigator: Mathhew Dr Callister, BM PhD|
|University College London Hospitals Nhs Foundation Trust||Recruiting|
|London, United Kingdom, NW1 2PG|
|Principal Investigator: Ashley Dr Groves, MBBS|
|University Hospital of South Manchester Nhs Foundation Trust||Recruiting|
|Manchester, United Kingdom, M23 9LT|
|Principal Investigator: Philip Dr Crosbie, PhD|
|Principal Investigator:||Steve George, MD,FRCP||University of Southampton|