Lung CancerPVD-LungsNCT07598279
Peripheral Vascular Disease as a Clinical Trigger for Opportunistic Lung Cancer Screening Referral: An Implementation Study
A study testing Observational - low dose computed tomography scan and Experimental - low dose computed tomography scan in people with Lung Cancer and Peripheral Vascular Diseases, run by International Agency for Research on Cancer at 1 site in India.
Trial summary
The study aims to determine whether patients with peripheral vascular disease who attend the vascular clinics are eligible for lung cancer screening. This is because long-term cigarette smoking exposure is associated with peripheral vascular disease, and smoking is again the main risk factor for lung cancer. Read more about this study
- Who is it for?
- Ages 40 to 80 years
- Conditions the study is for
- Lung Cancer, Peripheral Vascular Diseases, Ankle Brachial Index
- What is being tested?
- Observational - low dose computed tomography scan and Experimental - low dose computed tomography scan
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 355 participants
- Where
- 1 siteIndia
- Study dates
- 1 Jun 2026to Mar 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- All patients known/suspected to have peripheral vascular disease attending specified clinics in the tertiary care hospital
Who cannot join
- Prior diagnosis of lung cancer established/on work-up
- Patients with no smoking history
- Patients not eligible for low-dose CT scan
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
India1 site
Indira Gandhi Government General Hospital and Post Graduate Institute
Puducherry
Sidharth Parivallal, MS General Surgery, 0413-2336050, lakshmanasamyr@iarc.who.int
Sidharth Parivallal, MS General Surgery
About this study
Official title: Peripheral Vascular Disease as a Clinical Trigger for Opportunistic Lung Cancer Screening Referral: A Tertiary Care Implementation Study
The study aims to determine whether patients with peripheral vascular disease who attend the vascular clinics are eligible for lung cancer screening. This is because long-term cigarette smoking exposure is associated with peripheral vascular disease, and smoking is again the main risk factor for lung cancer.
These clinical encounters provide a potential opportunity to identify individuals who may qualify for lung cancer screening but are not routinely assessed for screening eligibility. Integrating systematic screening eligibility assessment within vascular clinics could therefore represent an effective strategy for identifying high-risk individuals and improving referral for lung cancer screening.
Read more
Additionally, peripheral arterial disease is commonly diagnosed using the ankle-brachial index (ABI), a non-invasive measure that compares systolic blood pressure between the ankle and brachial arteries. An ABI value below 0.90 is widely recognised as diagnostic of peripheral arterial disease and reflects the presence of systemic atherosclerosis.
ABI has been increasingly recognized as a marker of cumulative exposure to cardiovascular risk factors, particularly long-term tobacco smoking. Tobacco smoking contributes to endothelial dysfunction, chronic inflammation, and atherosclerotic plaque formation, mechanisms that are also implicated in lung carcinogenesis.
Because both lung cancer and peripheral vascular disease share major risk factors, ABI may serve as a clinical proxy indicator of cumulative smoking-related vascular damage. Individuals with lower ABI values may therefore represent a subgroup with higher cumulative tobacco exposure and potentially elevated lung cancer risk.
Evaluating the association between ABI severity categories and lung cancer diagnosis may provide insights into whether vascular disease severity could help identify individuals who may benefit from targeted screening interventions. If an association is observed, ABI could potentially be used as a simple, routinely measured clinical indicator to prompt lung cancer screening assessment in vascular care settings.
Therefore, this study will determine the proportion of the vascular disease patients who fall under the high-risk group for lung cancer screening and refer them to low-dose CT scan and follow-up them for the results and the adherence.
Read the detailed description
Primary Objective:
To estimate the proportion of patients with peripheral vascular disease eligible for and referred to lung cancer screening in a tertiary healthcare setting
Secondary Objectives:
- To assess the potential for expanded eligibility criteria for screening, by the inclusion of peripheral vascular disease as an additional risk stratification measure
- To quantify the distribution of smoking exposure(pack-years), ABI values, and other lung cancer risk factors in patients with peripheral vascular disease.
- To assess the association between ABI categories and the low-dose CT scan findings.
- To evaluate the feasibility of the risk-based lung cancer screening from vascular clinics in the tertiary care set-up using implementation science frameworks
Study design:
The investigators will conduct a prospective study among patients diagnosed with peripheral vascular disease at a tertiary care hospital. The investigators will assess lung cancer screening eligibility among these patients and the feasibility of implementing lung cancer screening for patients referred from the vascular clinics in the tertiary healthcare setting using RE-AIM implementation science framework.
Study population:
All individuals, aged 40 and above, diagnosed with a peripheral vascular disease in the surgical, medical and cardio-vascular OPDs in the tertiary care hospital.
Although current lung cancer screening recommendations generally target adults aged 50 years and older with substantial smoking exposure(20 pack-years), this study includes participants aged 40 years and above due to the presence of peripheral vascular disease (PVD), a condition strongly associated with long-term tobacco exposure and systemic atherosclerosis.
Peripheral vascular disease often manifests earlier than other smoking-related malignancies and may serve as a clinical marker of cumulative vascular and inflammatory damage related to chronic smoking.
Furthermore, the ankle-brachial index (ABI), an objective measure of peripheral arterial disease severity, reflects the burden of systemic atherosclerosis and long-term exposure to shared risk factors such as tobacco use, ageing, and chronic inflammation. Patients presenting with abnormal ABI values may therefore represent a risk-enriched subgroup in which earlier evaluation for lung cancer risk may be justified.
Including individuals aged 40 years and above allows this study to explore whether PVD and ABI abnormalities can function as additional clinical indicators to identify high-risk individuals who may otherwise fall outside conventional age-based screening thresholds. Additionally, the investigators will screen patients with pack-years 15 and above(and not quit in last 15 years), as they are already peripheral vascular disease patients and have considerable vascular damage.
Exclusion criteria:
- Prior diagnosis of lung cancer established/on work-up
- Patients with no smoking history
- Patients not eligible for low-dose CT scan
Study period:
The study period is June 2026- January 2027, with 6 months for recruitment of an adequate number of sample size with additional months for follow up of the set of individuals who were referred for low-dose CT scan lung cancer screening
Study Procedure:
The study will include all individuals diagnosed with a peripheral vascular disease, with age more than 40 years, in the surgical, cardio-vascular and medical outpatient departments in the hospital. The investigators will collect data on the socio-demographic profile and lung cancer-related history and co-morbidity details from these patients. The investigators will assess the eligibility for lung cancer screening in these individuals by calculating the smoking history (pack years). Further, the ankle-brachial index in these patients will be evaluated, as per the standard specifications. Patients who meet the criteria for lung cancer screening will be referred for low-dose computed tomography screening.
The lung cancer screening criteria, as prescribed by USPSTF: Individuals aged 50 to 80 years who have more than 20 pack-years of smoking history and currently smoke or have quit within the past 15 years will be the standard criteria for screening in this study. For this study purpose, since PVD is included as an additional condition, the investigators will screen participants who are more than 40 years old and those with pack years of 15 and above, and not quit in last 15 years in addition to the standard criteria, as a disease due to this major risk-factor is already established in them. This would be an expanded eligibility criteria for screening and forms the exploratory group in the study.
Patients who do not report to the LDCT appointment will be contacted by the research assistant up to 2 times with rescheduled dates. Reason for non-attendance will be noted. After the LDCT, those with lung lesions will be referred to the regional cancer centre for further management and follow-up to confirm the diagnosis.
Study setting:
The study will be conducted in the tertiary care district headquarters hospital. Out-patient departments which cater to peripheral vascular disease patients: Surgical, Medical and cardio-vascular departments will be involved for patient recruitment. However, patients will be assessed by the investigator from the surgical department, and the radiology department will offer the LDCT screening services for those referred from the surgical department, as part of the study.
Sample size:
The sample size has been calculated using eligibility for lung cancer screening as the outcome of interest. Assuming that 30% of the patients with a peripheral vascular disease will be eligible for lung cancer screening, and 95 percent confidence interval, the sample size is 323 participants. Considering a 10% non-response rate, 355 participants with peripheral vascular disease have to be recruited and assessed.
Outcomes:
The primary outcomes of the study will measure the proportion of peripheral vascular disease patients, found eligible for lung cancer screening (as per standard screening recommendations - USPSTF)
The secondary outcome indicators will measure the following:
- Proportion of patients found additionally eligible for the expanded screening eligibility
- Distribution and association of ABI with screening eligibility
- Proportion of patients with peripheral vascular disease assessed for lung cancer screening eligibility (Reach)
- Proportion of eligible patients referred for LDCT screening (Adoption)
- Proportion of referred patients who complete LDCT screening (Uptake)
- Proportion of screened participants with lung nodules or suspected malignancy (Detection Yield) - for standard and expanded LCS
- Conditions
- Lung Cancer, Peripheral Vascular Diseases, Ankle Brachial Index, Low Dose Computed Tomography
- Being tested
- Observational - low dose computed tomography scan, Experimental - low dose computed tomography scan
- Keywords
- lung cancer, peripheral vascular disease, ankle brachial index, low dose computed tomography, lung cancer screening, opportunistic screening
- Medical subject headings
- Lung Neoplasms, Peripheral Vascular Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Observational - low dose computed tomography scanProcedure or surgery
Low dose CT scan for the standard screening arm
Experimental - low dose computed tomography scanProcedure or surgery
low dose CT scan for the expanded screening group
| Study group | Role | What they receive |
|---|---|---|
| Standard screening protocol arm | Active comparator | Patients eligible as per the USPSTF high-risk age and smoking history Receives: Procedure: Observational - low dose computed tomography scan |
| Expanded screening group arm | Experimental | Patients with expanded high-risk group: beyond the USPSTF recommendation - 40 years age and above and those with more than 15 pack-years smoking history, not quit in last 15 years Receives: Procedure: Experimental - low dose computed tomography scan |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of peripheral vascular disease patients who are eligible for lung cancer screening (as per standard screening recommendations - USPSTF)
Measured: 6 months
Secondary outcomes (1)
Proportion of peripheral vascular disease patients who are screened for lung cancer by LDCT as per the expanded eligibility criteria
Expanded eligibility criteria as per the study includes individuals who are more than 40 years old and those with smoking pack years of 15 and above, and not quit in last 15 years
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 May 2026
- Study start1 Jun 2026 (estimated)
- Primary completionJan 2027 (estimated)
- Study completionMar 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lung CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 355 participants (estimated)
Sponsor and investigators
- Lead sponsor
- International Agency for Research on Cancer
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ravivarman Lakshmanasamy, International Agency for Research on Cancer
- Investigators
- Ravivarman LAKSHMANASAMY, Principal investigator, International Agency for Research on Cancer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07598279
- Sponsor's protocol ID
- PVD-Lungs
- Acronym
- PVD-Lungs
- Status last verified
- May 2026
- First submitted
- 1 May 2026
- Last updated
- 20 May 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 20 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Peripheral Vascular Disease as a Clinical Trigger for Opportunistic Lung Cancer Screening Referral: A Tertiary Care Implementation Study
- ClinicalTrials.gov ID
- NCT07598279
- Acronym / sponsor ID
- PVD-Lungs / PVD-Lungs
- Conditions
- Lung Cancer, Peripheral Vascular Diseases, Ankle Brachial Index, Low Dose Computed Tomography
- Keywords
- lung cancer, peripheral vascular disease, ankle brachial index, low dose computed tomography, lung cancer screening, opportunistic screening
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 355 participants (estimated)
- Lead sponsor
- International Agency for Research on CancerUniversity, hospital or other
- Study start
- 1 Jun 2026 (estimated)
- Primary completion
- Jan 2027 (estimated)
- Study completion
- Mar 2027 (estimated)
- First posted
- 20 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The study aims to determine whether patients with peripheral vascular disease who attend the vascular clinics are eligible for lung cancer screening. This is because long-term cigarette smoking exposure is associated with peripheral vascular disease, and smoking is again the main risk factor for lung cancer.
These clinical encounters provide a potential opportunity to identify individuals who may qualify for lung cancer screening but are not routinely assessed for screening eligibility. Integrating systematic screening eligibility assessment within vascular clinics could therefore represent an effective strategy for identifying high-risk individuals and improving referral for lung cancer screening.
Additionally, peripheral arterial disease is commonly diagnosed using the ankle-brachial index (ABI), a non-invasive measure that compares systolic blood pressure between the ankle and brachial arteries. An ABI value below 0.90 is widely recognised as diagnostic of peripheral arterial disease and reflects the presence of systemic atherosclerosis.
ABI has been increasingly recognized as a marker of cumulative exposure to cardiovascular risk factors, particularly long-term tobacco smoking. Tobacco smoking contributes to endothelial dysfunction, chronic inflammation, and atherosclerotic plaque formation, mechanisms that are also implicated in lung carcinogenesis.
Because both lung cancer and peripheral vascular disease share major risk factors, ABI may serve as a clinical proxy indicator of cumulative smoking-related vascular damage. Individuals with lower ABI values may therefore represent a subgroup with higher cumulative tobacco exposure and potentially elevated lung cancer risk.
Evaluating the association between ABI severity categories and lung cancer diagnosis may provide insights into whether vascular disease severity could help identify individuals who may benefit from targeted screening interventions. If an association is observed, ABI could potentially be used as a simple, routinely measured clinical indicator to prompt lung cancer screening assessment in vascular care settings.
Therefore, this study will determine the proportion of the vascular disease patients who fall under the high-risk group for lung cancer screening and refer them to low-dose CT scan and follow-up them for the results and the adherence.
Detailed description
Primary Objective:
To estimate the proportion of patients with peripheral vascular disease eligible for and referred to lung cancer screening in a tertiary healthcare setting
Secondary Objectives:
- To assess the potential for expanded eligibility criteria for screening, by the inclusion of peripheral vascular disease as an additional risk stratification measure
- To quantify the distribution of smoking exposure(pack-years), ABI values, and other lung cancer risk factors in patients with peripheral vascular disease.
- To assess the association between ABI categories and the low-dose CT scan findings.
- To evaluate the feasibility of the risk-based lung cancer screening from vascular clinics in the tertiary care set-up using implementation science frameworks
Study design:
The investigators will conduct a prospective study among patients diagnosed with peripheral vascular disease at a tertiary care hospital. The investigators will assess lung cancer screening eligibility among these patients and the feasibility of implementing lung cancer screening for patients referred from the vascular clinics in the tertiary healthcare setting using RE-AIM implementation science framework.
Study population:
All individuals, aged 40 and above, diagnosed with a peripheral vascular disease in the surgical, medical and cardio-vascular OPDs in the tertiary care hospital.
Although current lung cancer screening recommendations generally target adults aged 50 years and older with substantial smoking exposure(20 pack-years), this study includes participants aged 40 years and above due to the presence of peripheral vascular disease (PVD), a condition strongly associated with long-term tobacco exposure and systemic atherosclerosis.
Peripheral vascular disease often manifests earlier than other smoking-related malignancies and may serve as a clinical marker of cumulative vascular and inflammatory damage related to chronic smoking.
Furthermore, the ankle-brachial index (ABI), an objective measure of peripheral arterial disease severity, reflects the burden of systemic atherosclerosis and long-term exposure to shared risk factors such as tobacco use, ageing, and chronic inflammation. Patients presenting with abnormal ABI values may therefore represent a risk-enriched subgroup in which earlier evaluation for lung cancer risk may be justified.
Including individuals aged 40 years and above allows this study to explore whether PVD and ABI abnormalities can function as additional clinical indicators to identify high-risk individuals who may otherwise fall outside conventional age-based screening thresholds. Additionally, the investigators will screen patients with pack-years 15 and above(and not quit in last 15 years), as they are already peripheral vascular disease patients and have considerable vascular damage.
Exclusion criteria:
- Prior diagnosis of lung cancer established/on work-up
- Patients with no smoking history
- Patients not eligible for low-dose CT scan
Study period:
The study period is June 2026- January 2027, with 6 months for recruitment of an adequate number of sample size with additional months for follow up of the set of individuals who were referred for low-dose CT scan lung cancer screening
Study Procedure:
The study will include all individuals diagnosed with a peripheral vascular disease, with age more than 40 years, in the surgical, cardio-vascular and medical outpatient departments in the hospital. The investigators will collect data on the socio-demographic profile and lung cancer-related history and co-morbidity details from these patients. The investigators will assess the eligibility for lung cancer screening in these individuals by calculating the smoking history (pack years). Further, the ankle-brachial index in these patients will be evaluated, as per the standard specifications. Patients who meet the criteria for lung cancer screening will be referred for low-dose computed tomography screening.
The lung cancer screening criteria, as prescribed by USPSTF: Individuals aged 50 to 80 years who have more than 20 pack-years of smoking history and currently smoke or have quit within the past 15 years will be the standard criteria for screening in this study. For this study purpose, since PVD is included as an additional condition, the investigators will screen participants who are more than 40 years old and those with pack years of 15 and above, and not quit in last 15 years in addition to the standard criteria, as a disease due to this major risk-factor is already established in them. This would be an expanded eligibility criteria for screening and forms the exploratory group in the study.
Patients who do not report to the LDCT appointment will be contacted by the research assistant up to 2 times with rescheduled dates. Reason for non-attendance will be noted. After the LDCT, those with lung lesions will be referred to the regional cancer centre for further management and follow-up to confirm the diagnosis.
Study setting:
The study will be conducted in the tertiary care district headquarters hospital. Out-patient departments which cater to peripheral vascular disease patients: Surgical, Medical and cardio-vascular departments will be involved for patient recruitment. However, patients will be assessed by the investigator from the surgical department, and the radiology department will offer the LDCT screening services for those referred from the surgical department, as part of the study.
Sample size:
The sample size has been calculated using eligibility for lung cancer screening as the outcome of interest. Assuming that 30% of the patients with a peripheral vascular disease will be eligible for lung cancer screening, and 95 percent confidence interval, the sample size is 323 participants. Considering a 10% non-response rate, 355 participants with peripheral vascular disease have to be recruited and assessed.
Outcomes:
The primary outcomes of the study will measure the proportion of peripheral vascular disease patients, found eligible for lung cancer screening (as per standard screening recommendations - USPSTF)
The secondary outcome indicators will measure the following:
- Proportion of patients found additionally eligible for the expanded screening eligibility
- Distribution and association of ABI with screening eligibility
- Proportion of patients with peripheral vascular disease assessed for lung cancer screening eligibility (Reach)
- Proportion of eligible patients referred for LDCT screening (Adoption)
- Proportion of referred patients who complete LDCT screening (Uptake)
- Proportion of screened participants with lung nodules or suspected malignancy (Detection Yield) - for standard and expanded LCS
Study design
- Primary purpose
- Screening
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard screening protocol arm | Active comparator | Procedure: Observational - low dose computed tomography scanPatients eligible as per the USPSTF high-risk age and smoking history |
| Expanded screening group arm | Experimental | Procedure: Experimental - low dose computed tomography scanPatients with expanded high-risk group: beyond the USPSTF recommendation - 40 years age and above and those with more than 15 pack-years smoking history, not quit in last 15 years |
Who may qualify
- Ages
- 40 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- All patients known/suspected to have peripheral vascular disease attending specified clinics in the tertiary care hospital
Key exclusion criteria (3 listed)
- Prior diagnosis of lung cancer established/on work-up
- Patients with no smoking history
- Patients not eligible for low-dose CT scan
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Observational - low dose computed tomography scanLow dose CT scan for the standard screening arm | Procedure or surgery | Standard screening protocol arm |
| Experimental - low dose computed tomography scanlow dose CT scan for the expanded screening group | Procedure or surgery | Expanded screening group arm |
Primary outcome
Proportion of peripheral vascular disease patients who are eligible for lung cancer screening (as per standard screening recommendations - USPSTF)
Time frame: 6 months
1 secondary outcome
Proportion of peripheral vascular disease patients who are screened for lung cancer by LDCT as per the expanded eligibility criteria
Time frame: 6 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 May 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Indira Gandhi Government General Hospital and Post Graduate Institute
Puducherry, India
Ravivarman LAKSHMANASAMY principal investigator
International Agency for Research on Cancer
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Observational - low dose computed tomography scan and Experimental - low dose computed tomography scan in people with Lung Cancer and Peripheral Vascular Diseases, run by International Agency for Research on Cancer at 1 site in India.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 20 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in India. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Proportion of peripheral vascular disease patients who are eligible for lung cancer screening (as per standard screening recommendations - USPSTF) (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 May 2026.