Femoral Artery StenosisNCT05734157
CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Proximal Popliteal Artery
A study testing Peripheral PTA with a drug coated balloon in people with Femoral Artery Stenosis and Popliteal Artery Stenosis, run by Abbott Medical Devices at 8 sites in 2 countries.
Trial summary
The CVT-SFA Trial investigates the inhibition of restenosis using the CVT Everolimus-coated PTA Catheter in the treatment of de-novo occluded/ stenotic or re-occluded/restenotic superficial femoral or popliteal arteries. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Femoral Artery Stenosis, Popliteal Artery Stenosis, Femoral Artery Occlusion
- What is being tested?
- Peripheral PTA with a drug coated balloon
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 75 participants
- Where
- 8 sitesin 2 countries
- Study dates
- 17 Feb 2022to 27 Aug 2025
- Phase
- Interventional
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Subject must be at least 18 years of age.
- Subject or his/her legally authorized representative provides written informed consent prior to any clinical investigation related procedure, as approved by the appropriate Ethics Committee of the respective clinical site.
- Subject must agree to undergo all clinical investigation plan-required follow-up visits and examinations.
- Subjects with symptomatic leg ischemia, requiring treatment of SFA or popliteal (P1 segment) artery.
- De novo or restenotic lesion(s) >70% within the SFA and popliteal arteries in a single limb which are ≥3 cm and ≤15 cm in cumulative total length (by visual estimation). Lesion must be at least 2 cm from any stented area.
- Subject is willing to comply with the required follow up visits, testing schedule and medication regimen.
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- Successful wire crossing of lesion.
- Target vessel reference diameter ≥4 mm and ≤6 mm (by visual estimation).
- Target lesion(s) can be treated with a maximum of two (2) CVT Everolimus-coated PTA Catheters.
- At least one patent (less than 50% stenosis) tibio-peroneal run-off vessel confirmed by baseline angiography or prior MR angiography or CT angiography.
- Life expectancy >1 year
- Rutherford classification of 2, 3 or 4.
Who cannot join
- Pregnant or lactating females.
- Co-existing clinically significant aneurismal disease of the abdominal aorta, iliac or popliteal arteries.
- Significant gastrointestinal bleeding or any coagulopathy that would contraindicate the use of anti-platelet therapy.
- Known intolerance to study medications, everolimus or contrast agents.
- Doubts in the willingness or capability of the subject to allow follow-up examinations.
- Subject is actively participating in another investigational device or drug study.
Show all 19Show fewer
- History of hemorrhagic stroke within 3 months of procedure.
- Previous or planned surgical or interventional procedure within 30 days of index procedure.
- Prior vascular surgery of the target lesion.
- Lesion length is <3 cm or >15 cm or there is no normal proximal arterial segment in which duplex ultrasound velocity ratios can be measured.
- Known inadequate distal outflow.
- Significant inflow disease.
- Acute or sub-acute thrombus in target vessel.
- Use of adjunctive therapies (i.e. laser, atherectomy, cryoplasty, scoring/cutting balloons, brachytherapy, lithotripsy).
- Outflow arteries (distal popliteal, anterior or posterior tibial or peroneal arteries) with significant lesions (≥ 50% stenosis) may not be treated during the same procedure.
- Treatment of the contralateral limb during the same procedure or within 30 days of the study procedure.
- Rutherford classification of 0, 1, 5 or 6
- Presence of prohibitive calcification that precludes adequate PTA treatment.
- Subjects held in custody in an institution by official or court order.
Trial locations and contacts
8 sites in 2 countries.
8 sites in 2 countries
France4 sites
Polyclinique Les Fleurs
Ollioules, 83190
Hôpital Paris Saint Joseph
Paris, 75014
Hôpital Nord Laennec - CHU de Nantes
Saint-Herblain, 44800
Clinique Pasteur
Toulouse, 31300
Germany4 sites
Institut für Radiologie, Kinderradiologie und interventionelle Therapie
Berlin, 12351
Jüdisches Krankenhaus Berlin
Berlin, 13347
DIAKO Krankenhaus Flensburg
Flensburg, 24939
Romed Klinikum Rosenheim
Rosenheim, 83022
About this study
Official title: Chansu Vascular Technologies Everolimus-Coated Balloon Percutaneous Transluminal Angioplasty Catheter First-in-Human Clinical Investigation
The CVT-SFA Trial investigates the inhibition of restenosis using the CVT Everolimus-coated PTA Catheter in the treatment of de-novo occluded/ stenotic or re-occluded/restenotic superficial femoral or popliteal arteries.
Read the detailed description
The CVT-SFA Trial is a prospective, multi-center, open, single arm study enrolling subjects with de-novo or post-PTA occluded/stenotic or re-occluded/ restenotic lesions (excluding in-stent lesions) ≤150mm in length in femoropopliteal arteries with reference vessel diameters of 4-6mm, receiving up to two (2) CVT Everolimus-coated PTA Catheters to establish blood flow and to maintain vessel patency.
- Conditions
- Femoral Artery Stenosis, Popliteal Artery Stenosis, Femoral Artery Occlusion, Popliteal Artery Occlusion
- Being tested
- Peripheral PTA with a drug coated balloon
- Keywords
- TP1109, CVT-SFA, Femoral Artery Stenosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Peripheral PTA with a drug coated balloonDevice
Peripheral artery angioplasty
| Study group | Role | What they receive |
|---|---|---|
| Everolimus-coated balloon | Experimental | Treatment of patients with de-novo or post-PTA occluded/stenotic or re-occluded/restenotic lesions in femoropopliteal arteries with a drug-coated balloon. Receives: Device: Peripheral PTA with a drug coated balloon |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number and Percentage of Participants With Freedom of Major Adverse Event (MAE) Rate
Freedom from MAEs defined as a composite rate of cardiovascular death, index limb amputation, and ischemia-driven TLR.
Measured: 6 months post procedure
The Primary Effectiveness Endpoint: Patency (Freedom From Restenosis, Freedom From Ischemia-driven TLR)
Freedom from restenosis as determined by duplex ultrasonography (DUS) (peak systolic velocity ratio (PSVR) ≤2.4 or ≤50% stenosis) and freedom from ischemia-driven target lesion revascularization (TLR).
Measured: 6 months post procedure
Secondary outcomes (28)
Rate of Major Adverse Event (MAE)
Composite rate of cardiovascular death, index limb amputation and ischemia-driven Target Lesion Revascularization (TLR). The time frame for "In hospital" refers to time from procedure to discharge. This timeframe is different for every enrolled subject. The subject is discharged at the treating physician's discretion based on their specific treatment needs.
Measured: In Hospital
Rate of Major Adverse Event (MAE)
Composite rate of cardiovascular death, index limb amputation and ischemia-driven Target Lesion Revascularization (TLR).
Measured: 30 Days Post-procedure
Rate of Major Adverse Event (MAE)
Composite rate of cardiovascular death, index limb amputation and ischemia-driven Target Lesion Revascularization (TLR).
Measured: 12 months Post-procedure
Rate of Major Adverse Event (MAE)
Composite rate of cardiovascular death, index limb amputation and ischemia-driven Target Lesion Revascularization (TLR).
Measured: 24months
Rate of Major Adverse Event (MAE)
Composite rate of cardiovascular death, index limb amputation and ischemia-driven Target Lesion Revascularization (TLR).
Measured: 36months
Rate of Occurrence of Arterial Thrombosis of the Treated Segment
Rate of occurrence arterial thrombosis of the treated segment as determined by QVA
Measured: 12months
Rate of Ipsilateral Embolic Events of the Study Limb
This end point was to asses the Rate of Ipsilateral Embolic Events of the Study Limb.
Measured: 12 months
Rate of Clinically-driven Target Lesion Revascularization
This end point was to asses the Rate of Clinically-driven Revascularization.
Measured: 6 months
Rate of Clinically-driven Target Lesion Revascularization
This end point was to asses the Rate of Clinically-driven Revascularization.
Measured: 12 months
Rate of Clinically-driven Target Lesion Revascularization
This end point was to asses the Rate of Clinically-driven Revascularization.
Measured: 24 months
Rate of Clinically-driven Target Lesion Revascularization
This end point was to asses the Rate of Clinically-driven Revascularization.
Measured: 36 months
Patency Rate
The patency results achieved in the CVT-SFA Study translate into meaningful patient benefits as demonstrated by the improvement of secondary outcomes measures.
Measured: 12 months
Rate of Vascular Access Site Complication
Rate of vascular access site complication defined as the combined rate of hematoma, AV fistula or a pseudoaneurysm that required intervention, such as surgical repair or transfusion, prolonged hospital stay, or required a new hospital admission.
Measured: 12 months
Lesion Success
Lesion success (per device), defined as achievement of a final in-lesion residual diameter stenosis of <50% (by QA), using any device after wire passage through the lesion. Pre- and post-dilatation of the lesion with a non-study device is considered part of assigned device treatment.
Measured: 12 months
Technical Success
Technical success (per device), defined as achievement of a final in-lesion residual diameter stenosis of <50% (by QA), using the CVT Everolimus-coated PTA Catheter without a device malfunction after wire passage through the lesion. Pre- and postdilatation are considered part of assigned device treatment.
Measured: 12 months
Clinical Success
Clinical success (per subject) defined as technical success without the occurrence of major adverse events (MAE) during the procedure.
Measured: 12 months
Procedural Success
Procedural success (per subject) defined as lesion success without the occurrence of major adverse events during procedure.
Measured: 12 months
Change in Ankle-Brachial Index (ABI)
Change in Ankle-Brachial Index (ABI) is calculated as the difference between the ABI values at baseline and at follow-up visits. ABI is measured using a Doppler ultrasound or Oscillo metric method to assess peripheral arterial function. A change of ≥0.1 in ABI values from baseline to follow-up is considered clinically significant. The data presented in the Outcome Measure table reflects the percentage of participants who experienced a significant change in ABI from baseline.
Measured: Discharge
Change in Ankle-Brachial Index (ABI)
Change in Ankle-Brachial Index (ABI) is calculated as the difference between the ABI values at baseline and at follow-up visits. ABI is measured using a Doppler ultrasound or Oscillo metric method to assess peripheral arterial function. A change of ≥0.1 in ABI values from baseline to follow-up is considered clinically significant. The data presented in the Outcome Measure table reflects the percentage of participants who experienced a significant change in ABI from baseline.
Measured: 6 months
Change in Ankle-Brachial Index (ABI)
Change in Ankle-Brachial Index (ABI) is calculated as the difference between the ABI values at baseline and at follow-up visits. ABI is measured using a Doppler ultrasound or Oscillo metric method to assess peripheral arterial function. A change of ≥0.1 in ABI values from baseline to follow-up is considered clinically significant. The data presented in the Outcome Measure table reflects the percentage of participants who experienced a significant change in ABI from baseline.
Measured: 12 months
Walking Impairment Questionnaire - Patient Perceived Change in Walking Difficulty
The WIQ (Walking Impairment Questionnaire) score is a numerical representation of a person's walking capacity, derived from their responses to a series of questions about walking difficulty. Individuals are asked to rate degree of difficulty of various activities with responses ranging from 0 (lowest possible function) to 4 (highest possible function). Questions within each category are based on degree of difficulty, according to approximate number of feet, stairs, or miles per hour for distance, stair-climbing, and speed scores, respectively. Scores are then divided by maximum number of points and presented on a scale of 0% to 100%, where 0% represents lowest possible score (i.e., answering "unable" for all questions in that category) and 100% represents the highest possible score (i.e., indicating "none" with regard to difficulty for all questions in that category). A higher score indicates less difficulty with walking, while a lower score signifies greater difficulty with walking.
Measured: Pre-Procedure to 6 months and 12 months
Walking Impairment Questionnaire - Patient Perceived Change in Walking Speed
The WIQ (Walking Impairment Questionnaire) score is a numerical representation of a person's walking capacity, derived from their responses to a series of questions about walking difficulty. Individuals are asked to rate the degree of difficulty of various activities with responses ranging from 0 (lowest possible function) to 4 (highest possible function). Questions within each category are based on the degree of difficulty, according to the approximate number of feet, stairs, or miles per hour for the distance, stair-climbing, and speed scores, respectively. Scores are then divided by the maximum number of points and presented on a scale of 0% to 100%, where 0%represents the lowest possible score (i.e., answering "unable" for all questions in that category) and 100% represents the highest possible score (i.e., indicating "none" with regard to difficulty for all questions in that category). Higher scores signify less difficulty in maintaining speed while walking.
Measured: Pre-Procedure to 6 months and 12 months
Walking Impairment Questionnaire - Patient Perceived Change in Walking Impairment
The WIQ (Walking Impairment Questionnaire) score is a numerical representation of a person's walking capacity, derived from their responses to a series of questions about walking difficulty. Individuals are asked to rate the degree of difficulty of various activities with responses ranging from 0 (lowest possible function) to 4 (highest possible function). Questions within each category are based on the degree of difficulty, according to the approximate number of feet, stairs, or miles per hour for the distance, stair-climbing, and speed scores, respectively. Scores are then divided by the maximum number of points and presented on a scale of 0% to 100%, where 0%represents the lowest possible score (i.e., answering "unable" for all questions in that category) and 100% represents the highest possible score (i.e., indicating "none" with regard to difficulty for all questions in that category). A higher score indicates less perceived walking impairment.
Measured: Pre-Procedure to 6 months and 12 months
Walking Test: Change in Walking Distance
The Walking Test is a standard test used to evaluate functionality in patients with peripheral artery disease (PAD). This test measures the distance that a patient can quickly walk on a flat, hard surface in a period of 6 minutes.
Measured: Baseline to 6 months and 12 months
Treadmill Test: Change in Walking Distance
Treadmill walking test is a standard test used to evaluate functionality in patients with peripheral artery disease (PAD).
Measured: Baseline to 6 months and 12 months
Change in Rutherford Classification
Participants were graded using the Rutherford Classification, which stages PAD based on symptoms and clinical findings.
Class 0 asymptomatic , normal treadmill or reactive hyperemia test. Class 1 mild claudication completes treadmill exercise; AP after exercise > 50 mm Hg but at least 20 mm Hg lower than resting value.
Class 2-3 more severe symptoms cannot complete standard treadmill exercise, and AP after exercise < 50 mm Hg.
Class 4 critical limb ischemia resting AP < 40 mm Hg, flat or barely pulsatile ankle or metatarsal PVR; TP < 30 mm Hg.
Class 5 minor tissue loss-nonhealing ulcer, focal gangrene with diffuse pedal ischemia and resting AP < 60 mm Hg, ankle or metatarsal PVR flat or barely pulsatile; TP < 40 mm Hg. The lower the RB Class the better the outcome.
Measured: Pre-procedure
Change in Rutherford Classification
Participants were graded using the Rutherford Classification, which stages PAD based on symptoms and clinical findings.
Class 0 asymptomatic , normal treadmill or reactive hyperemia test. Class 1 mild claudication completes treadmill exercise; AP after exercise > 50 mm Hg but at least 20 mm Hg lower than resting value.
Class 2-3 more severe symptoms cannot complete standard treadmill exercise, and AP after exercise < 50 mm Hg.
Class 4 critical limb ischemia resting AP < 40 mm Hg, flat or barely pulsatile ankle or metatarsal PVR; TP < 30 mm Hg.
Class 5 minor tissue loss-nonhealing ulcer, focal gangrene with diffuse pedal ischemia and resting AP < 60 mm Hg, ankle or metatarsal PVR flat or barely pulsatile; TP < 40 mm Hg. The lower the RB Class the better the outcome.
Measured: 6 months
Change in Rutherford Classification
Participants were graded using the Rutherford Classification, which stages PAD based on symptoms and clinical findings.
Class 0 asymptomatic , normal treadmill or reactive hyperemia test. Class 1 mild claudication completes treadmill exercise; AP after exercise > 50 mm Hg but at least 20 mm Hg lower than resting value.
Class 2-3 more severe symptoms cannot complete standard treadmill exercise, and AP after exercise < 50 mm Hg.
Class 4 critical limb ischemia resting AP < 40 mm Hg, flat or barely pulsatile ankle or metatarsal PVR; TP < 30 mm Hg.
Class 5 minor tissue loss-nonhealing ulcer, focal gangrene with diffuse pedal ischemia and resting AP < 60 mm Hg, ankle or metatarsal PVR flat or barely pulsatile; TP < 40 mm Hg. The lower the RB Class the better the outcome.
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Feb 2023
- Study start17 Feb 2022
- Primary completion11 Sep 2023
- Study completion27 Aug 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Femoral Artery StenosisStudies of the same condition, open and under way.
- More trials run by Abbott Medical DevicesThe sponsor's other registered studies.
- 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
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 75 participants (actual)
Sponsor and investigators
- Lead sponsor
- Abbott Medical Devices
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05734157
- Sponsor's protocol ID
- TP1109
- Status last verified
- May 2026
- First submitted
- 27 Jan 2023
- Last updated
- 13 May 2026
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 13 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Chansu Vascular Technologies Everolimus-Coated Balloon Percutaneous Transluminal Angioplasty Catheter First-in-Human Clinical Investigation
- ClinicalTrials.gov ID
- NCT05734157
- Acronym / sponsor ID
- TP1109
- Conditions
- Femoral Artery Stenosis, Popliteal Artery Stenosis, Femoral Artery Occlusion, Popliteal Artery Occlusion
- Keywords
- TP1109, CVT-SFA, Femoral Artery Stenosis
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 75 participants (actual)
- Lead sponsor
- Abbott Medical DevicesIndustry (pharma, biotech, devices)
- Study start
- 17 Feb 2022 (actual)
- Primary completion
- 11 Sep 2023 (actual)
- Study completion
- 27 Aug 2025 (actual)
- First posted
- 17 Feb 2023 (actual)
- Results
- Posted 7 Aug 2025
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The CVT-SFA Trial investigates the inhibition of restenosis using the CVT Everolimus-coated PTA Catheter in the treatment of de-novo occluded/ stenotic or re-occluded/restenotic superficial femoral or popliteal arteries.
Detailed description
The CVT-SFA Trial is a prospective, multi-center, open, single arm study enrolling subjects with de-novo or post-PTA occluded/stenotic or re-occluded/ restenotic lesions (excluding in-stent lesions) ≤150mm in length in femoropopliteal arteries with reference vessel diameters of 4-6mm, receiving up to two (2) CVT Everolimus-coated PTA Catheters to establish blood flow and to maintain vessel patency.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Everolimus-coated balloon | Experimental | Device: Peripheral PTA with a drug coated balloonTreatment of patients with de-novo or post-PTA occluded/stenotic or re-occluded/restenotic lesions in femoropopliteal arteries with a drug-coated balloon. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (12 listed)
- Subject must be at least 18 years of age.
- Subject or his/her legally authorized representative provides written informed consent prior to any clinical investigation related procedure, as approved by the appropriate Ethics Committee of the respective clinical site.
- Subject must agree to undergo all clinical investigation plan-required follow-up visits and examinations.
- Subjects with symptomatic leg ischemia, requiring treatment of SFA or popliteal (P1 segment) artery.
- De novo or restenotic lesion(s) >70% within the SFA and popliteal arteries in a single limb which are ≥3 cm and ≤15 cm in cumulative total length (by visual estimation). Lesion must be at least 2 cm from any stented area.
Key exclusion criteria (19 listed)
- Pregnant or lactating females.
- Co-existing clinically significant aneurismal disease of the abdominal aorta, iliac or popliteal arteries.
- Significant gastrointestinal bleeding or any coagulopathy that would contraindicate the use of anti-platelet therapy.
- Known intolerance to study medications, everolimus or contrast agents.
- Doubts in the willingness or capability of the subject to allow follow-up examinations.
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 |
|---|---|---|
| Peripheral PTA with a drug coated balloonPeripheral artery angioplasty | Device | Everolimus-coated balloon |
Primary outcome
Number and Percentage of Participants With Freedom of Major Adverse Event (MAE) Rate
Time frame: 6 months post procedure
Freedom from MAEs defined as a composite rate of cardiovascular death, index limb amputation, and ischemia-driven TLR.
The Primary Effectiveness Endpoint: Patency (Freedom From Restenosis, Freedom From Ischemia-driven TLR)
Time frame: 6 months post procedure
Freedom from restenosis as determined by duplex ultrasonography (DUS) (peak systolic velocity ratio (PSVR) ≤2.4 or ≤50% stenosis) and freedom from ischemia-driven target lesion revascularization (TLR).
28 secondary outcomes
Rate of Major Adverse Event (MAE)
Time frame: In Hospital
Rate of Major Adverse Event (MAE)
Time frame: 30 Days Post-procedure
Rate of Major Adverse Event (MAE)
Time frame: 12 months Post-procedure
Rate of Major Adverse Event (MAE)
Time frame: 24months
Rate of Major Adverse Event (MAE)
Time frame: 36months
Rate of Occurrence of Arterial Thrombosis of the Treated Segment
Time frame: 12months
Rate of Ipsilateral Embolic Events of the Study Limb
Time frame: 12 months
Rate of Clinically-driven Target Lesion Revascularization
Time frame: 6 months
Rate of Clinically-driven Target Lesion Revascularization
Time frame: 12 months
Rate of Clinically-driven Target Lesion Revascularization
Time frame: 24 months
Rate of Clinically-driven Target Lesion Revascularization
Time frame: 36 months
Patency Rate
Time frame: 12 months
Rate of Vascular Access Site Complication
Time frame: 12 months
Lesion Success
Time frame: 12 months
Technical Success
Time frame: 12 months
Clinical Success
Time frame: 12 months
Procedural Success
Time frame: 12 months
Change in Ankle-Brachial Index (ABI)
Time frame: Discharge
Change in Ankle-Brachial Index (ABI)
Time frame: 6 months
Change in Ankle-Brachial Index (ABI)
Time frame: 12 months
Walking Impairment Questionnaire - Patient Perceived Change in Walking Difficulty
Time frame: Pre-Procedure to 6 months and 12 months
Walking Impairment Questionnaire - Patient Perceived Change in Walking Speed
Time frame: Pre-Procedure to 6 months and 12 months
Walking Impairment Questionnaire - Patient Perceived Change in Walking Impairment
Time frame: Pre-Procedure to 6 months and 12 months
Walking Test: Change in Walking Distance
Time frame: Baseline to 6 months and 12 months
Treadmill Test: Change in Walking Distance
Time frame: Baseline to 6 months and 12 months
Change in Rutherford Classification
Time frame: Pre-procedure
Change in Rutherford Classification
Time frame: 6 months
Change in Rutherford Classification
Time frame: 12 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 May 2026.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: No
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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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
8 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Peripheral PTA with a drug coated balloon in people with Femoral Artery Stenosis and Popliteal Artery Stenosis, run by Abbott Medical Devices at 8 sites in 2 countries.
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 12 inclusion and 19 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: finished, as of the sponsor's last update on 13 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 8 sites in France, Germany. 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?
Yes. Results are posted in the registry (first posted 7 Aug 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number and Percentage of Participants With Freedom of Major Adverse Event (MAE) Rate (time frame: 6 months post procedure). The study lists 2 primary outcomes in all. 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 13 May 2026.