Critical Limb Ischemia (CLI)CLEAR TOENCT07014072
Comprehensive Limb Evaluation and Arterial Revascularization With Toe Pressure Optimization Registry
A study testing intensive toe pressure evaluation and data collection in people with Critical Limb Ischemia (CLI), run by University Hospital, Bordeaux at 1 site in France.
Trial summary
To address the heterogeneity of practices, better understand the outcomes of cricital limb theatening ischemia (CLTI) patients after endovascular interventions, and recognize effective endovascular options for infrapopliteal artery revascularization in CLTI, our prospective registry aims to tackle the critical… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Critical Limb Ischemia (CLI)
- What is being tested?
- intensive toe pressure evaluation and data collection
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 200 participants
- Where
- 1 siteFrance
- Study dates
- 7 Jul 2025to 30 Nov 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age ≥ 18 years
- Rutherford category 4 or 5
- Wounds limited to toes or forefoot with a salvageable limb
- Infrapopliteal lesions (infra-popliteal arteries) with >70% stenosis upon visual assessment during initial angiography
Who cannot join
- Previous or planned major amputation of the target limb
- Untreated aortoiliac/femoropopliteal stenotic disease limiting flow
- History of infrapopliteal bypass on the target limb
- Failure of percutaneous transluminal angioplasty of the target limb (technical failure)
- Absence of angiographic evidence of a patent artery below the ankle ("desert foot")
- Lesions located inside or near an arterial aneurysm
Show all 9Show fewer
- Life expectancy < 1 year
- Acute limb ischemia
- Septicemia or bacteremia
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site
Centre Hospitalier Universitaire de Bordeaux
Bordeaux, 33000
Eric DUCASSE, MD, PhD, +335 56 79 55 25, eric.ducasse@chu-bordeaux.fr
Olivier DELORME, +335 57 82 01 34, olivier.delorme@chu-bordeaux.fr
About this study
To address the heterogeneity of practices, better understand the outcomes of cricital limb theatening ischemia (CLTI) patients after endovascular interventions, and recognize effective endovascular options for infrapopliteal artery revascularization in CLTI, our prospective registry aims to tackle the critical question of whether intensive toe pressure evaluation, guiding repeat revascularization using predetermined thresholds (<30 mmHg or decrease >10% from immediate postoperative assessment), could optimize outcomes in patients with CLTI.
Read the detailed description
Cricital limb theatening ischemia (CLTI) represents the most advanced stage of peripheral arterial disease (PAD), leading to high mortality rates and limb loss. A primary endovascular strategy is now preferred for most patients with CLTI who have occlusive disease of the tibial arteries. This is especially true for the elderly, diabetic patients, and those without suitable venous conduits for bypass. Patients with CLTI and infra-popliteal occlusive disease do not always respond well to the provided treatment, but the underlying reasons, particularly in those showing good initial results after endovascular revascularization, remain to be determined.
The literature strongly supports the use of drug-eluting stents (DES) in treating infrapopliteal arteries. DES are associated with significant improvements in patency, reduced rates of restenosis and reintervention, and better Rutherford-Becker classification and healing of trophic disorders. However, contrary to initial expectations, the SAVAL trial, whose data were made public in December 2023, comparing a DES dedicated to infra-popliteal arteries with percutaneous transluminal angioplasty in patients with CLTI, failed to meet its primary efficacy (increased primary patency and reduced major adverse events rate) and safety objectives at 12 months, despite preliminary data suggesting an advantage in using DES for treating short lesions. A possible explanation is the significant heterogeneity of practices, with less than half of the patients receiving optimal medical treatment and intensive follow-up, highlighting the need for a comprehensive review of treatment strategies in this challenging patient population.
The lack of an established objective follow-up protocol for this patient group underscores the need for innovative approaches. Currently, there is no widely available consensus indicator to estimate whether the revascularization provided will be sufficient to prevent amputation. The Delta-Perf study has completed its recruitment and is expected to provide results on foot perfusion analysis in patients with CLTI before and after revascularization and its predictive value on amputation-free survival. However, despite high initial technical success rates for endovascular interventions, early failure of these minimally invasive procedures is common.
Current recommendations support duplex scan monitoring and prophylactic reintervention for asymptomatic graft stenosis to promote long-term patency, but monitoring and reintervention strategies after endovascular management have been left to the practitioner's discretion. There are no ongoing studies to determine if the initial improvement observed in the foot is actually maintained, and there is little evidence to support indications for repeated interventions in CLTI. Clinical follow-up alone may be insufficient to detect restenosis, as patients may remain asymptomatic until the target artery is occluded, similar to venous grafts in bypasses. Likewise, measuring the ankle-brachial index (ABI) alone has limited value, given the difficulty in determining the level of restenosis, technical limitations in diabetic patients with calcified vessels, and variability in correlation with the severity of lesions.
It is likely that there are subgroups of patients who could benefit more than others from early reintervention. Toe pressure, in this context, offers a measurable, non-invasive, and clinically relevant parameter that can be consistently evaluated even in challenging cases, particularly in heavily calcified patients.
- Conditions
- Critical Limb Ischemia (CLI)
- Being tested
- intensive toe pressure evaluation, data collection
- Keywords
- CLTI, toe pressure, limb salvage, endovascular revascularization, theatening
- Medical subject headings
- Chronic Limb-Threatening Ischemia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
intensive toe pressure evaluationProcedure or surgery
This measurement is non-invasive, painless and is also carried out as part of the care in the follow-up of critical limb ischemia. It takes place like a blood pressure measurement except that it is carried out at the level of a toe.
data collectionOther
retrospective data
| Study group | Role | What they receive |
|---|---|---|
| Historical cohort | Sham comparator | 100 patients with CLTI treated in the past 3 years at the same center. Patients in this cohort were treated according to standard clinical practices at the time, without intensive toe pressure evaluation to guide reinterventions, and with reinterventions guided solely by clinical criteria. Receives: Other: data collection |
| Prospective cohort | Experimental | 100 patients included prospectively and treated as part of the study. Patients in this cohort will be followed with an intensive toe pressure evaluation approach (TcPO2), guiding reinterventions according to predetermined thresholds (<30 mmHg or decrease >10% from immediate postoperative assessment). This cohort will receive best medical treatment: Receives: Procedure: intensive toe pressure evaluation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Toe pressure with Systolic pressure measurement device
The Systolic pressure measurement device is suitable for the toes, as part of the diagnosis or monitoring of obliterating arteriopathy of the lower limbs, as for the fingers of the hand during assessments relating to arteriovenous fistulas.
The Systolic pressure measurement device ingeniously uses photoplethysmography (PPG) associated with a unique algorithm developed and patented by Atys Medical. PPG makes it possible to detect, thanks to a photoelectric cell (sensor), variations in blood flow in skin traffic.
The Systolic pressure measurement deviceputs the measurement of digital pressure pressure within the reach of all the stakeholders concerned (angiologists, nephrologists, diabetologists, vascular surgeons, wound and healing services, etc.).
Measured: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Secondary outcomes (6)
Evaluation of Survival
Describe if patient is alive or not
Measured: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of the absence of target lesion occlusion.
Evaluation of absence of occlusion of the target lesion by Echo-doppler
Measured: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of target lesion revascularization
Evaluation of target lesion revascularization using Echo doppler
Measured: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of major adverse limb events
Evaluation of major amputation or major reinterventions including new bypass surgery, bypass revision, or thrombectomy/thrombolysis related to the target lesion
Measured: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation ofthe Wound healing with WiFi classification
It takes into account the patient's foot wound, ischemia and infection. This system can be used to determine the estimated 1-year risk of amputation and the estimated probability of benefit/need for revascularization. It is a useful, standardized tool that can help determine patient risk and the need for intervention.
Measured: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of the Wound healing with colorimetry scale
Colorimetry involves analyzing the different colors present in a wound to determine its condition and stage of healing. Each color corresponds to a specific tissue or biological process.
Measured: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jun 2025
- Study start7 Jul 2025 (estimated)
- Primary completion7 Jul 2027 (estimated)
- Study completion30 Nov 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Critical Limb Ischemia (CLI)Studies 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
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Bordeaux
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Eric DUCASSE, MD, PhD, Principal investigator, University Hospital, Bordeaux
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07014072
- Sponsor's protocol ID
- CHUBX 2025/006
- Other IDs
- 2025-A00272-47
- Acronym
- CLEAR TOE
- Status last verified
- May 2025
- First submitted
- 21 May 2025
- Last updated
- 10 Jun 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The data is available from Pr DUACSSE. An email can be sent to her so that she can contact the data manager and owner, the Bordeaux University Hospital. The data can be made available after contractual agreement
Study at a glance
From the registry record, last updated by the sponsor on 10 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comprehensive Limb Evaluation and Arterial Revascularization With Toe Pressure Optimization Registry
- ClinicalTrials.gov ID
- NCT07014072
- Acronym / sponsor ID
- CLEAR TOE / CHUBX 2025/006
- Conditions
- Critical Limb Ischemia (CLI)
- Keywords
- CLTI, toe pressure, limb salvage, endovascular revascularization, theatening
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- University Hospital, BordeauxUniversity, hospital or other
- Study start
- 7 Jul 2025 (estimated)
- Primary completion
- 7 Jul 2027 (estimated)
- Study completion
- 30 Nov 2027 (estimated)
- First posted
- 10 Jun 2025 (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.
To address the heterogeneity of practices, better understand the outcomes of cricital limb theatening ischemia (CLTI) patients after endovascular interventions, and recognize effective endovascular options for infrapopliteal artery revascularization in CLTI, our prospective registry aims to tackle the critical question of whether intensive toe pressure evaluation, guiding repeat revascularization using predetermined thresholds (<30 mmHg or decrease >10% from immediate postoperative assessment), could optimize outcomes in patients with CLTI.
Detailed description
Cricital limb theatening ischemia (CLTI) represents the most advanced stage of peripheral arterial disease (PAD), leading to high mortality rates and limb loss. A primary endovascular strategy is now preferred for most patients with CLTI who have occlusive disease of the tibial arteries. This is especially true for the elderly, diabetic patients, and those without suitable venous conduits for bypass. Patients with CLTI and infra-popliteal occlusive disease do not always respond well to the provided treatment, but the underlying reasons, particularly in those showing good initial results after endovascular revascularization, remain to be determined.
The literature strongly supports the use of drug-eluting stents (DES) in treating infrapopliteal arteries. DES are associated with significant improvements in patency, reduced rates of restenosis and reintervention, and better Rutherford-Becker classification and healing of trophic disorders. However, contrary to initial expectations, the SAVAL trial, whose data were made public in December 2023, comparing a DES dedicated to infra-popliteal arteries with percutaneous transluminal angioplasty in patients with CLTI, failed to meet its primary efficacy (increased primary patency and reduced major adverse events rate) and safety objectives at 12 months, despite preliminary data suggesting an advantage in using DES for treating short lesions. A possible explanation is the significant heterogeneity of practices, with less than half of the patients receiving optimal medical treatment and intensive follow-up, highlighting the need for a comprehensive review of treatment strategies in this challenging patient population.
The lack of an established objective follow-up protocol for this patient group underscores the need for innovative approaches. Currently, there is no widely available consensus indicator to estimate whether the revascularization provided will be sufficient to prevent amputation. The Delta-Perf study has completed its recruitment and is expected to provide results on foot perfusion analysis in patients with CLTI before and after revascularization and its predictive value on amputation-free survival. However, despite high initial technical success rates for endovascular interventions, early failure of these minimally invasive procedures is common.
Current recommendations support duplex scan monitoring and prophylactic reintervention for asymptomatic graft stenosis to promote long-term patency, but monitoring and reintervention strategies after endovascular management have been left to the practitioner's discretion. There are no ongoing studies to determine if the initial improvement observed in the foot is actually maintained, and there is little evidence to support indications for repeated interventions in CLTI. Clinical follow-up alone may be insufficient to detect restenosis, as patients may remain asymptomatic until the target artery is occluded, similar to venous grafts in bypasses. Likewise, measuring the ankle-brachial index (ABI) alone has limited value, given the difficulty in determining the level of restenosis, technical limitations in diabetic patients with calcified vessels, and variability in correlation with the severity of lesions.
It is likely that there are subgroups of patients who could benefit more than others from early reintervention. Toe pressure, in this context, offers a measurable, non-invasive, and clinically relevant parameter that can be consistently evaluated even in challenging cases, particularly in heavily calcified patients.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Historical cohort | Sham comparator | Other: data collection100 patients with CLTI treated in the past 3 years at the same center. Patients in this cohort were treated according to standard clinical practices at the time, without intensive toe pressure evaluation to guide reinterventions, and with reinterventions guided solely by clinical criteria. |
| Prospective cohort | Experimental | Procedure: intensive toe pressure evaluation100 patients included prospectively and treated as part of the study. Patients in this cohort will be followed with an intensive toe pressure evaluation approach (TcPO2), guiding reinterventions according to predetermined thresholds (<30 mmHg or decrease >10% from immediate postoperative assessment). This cohort will receive best medical treatment: |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Age ≥ 18 years
- Rutherford category 4 or 5
- Wounds limited to toes or forefoot with a salvageable limb
- Infrapopliteal lesions (infra-popliteal arteries) with >70% stenosis upon visual assessment during initial angiography
Key exclusion criteria (9 listed)
- Previous or planned major amputation of the target limb
- Untreated aortoiliac/femoropopliteal stenotic disease limiting flow
- History of infrapopliteal bypass on the target limb
- Failure of percutaneous transluminal angioplasty of the target limb (technical failure)
- Absence of angiographic evidence of a patent artery below the ankle ("desert foot")
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 |
|---|---|---|
| intensive toe pressure evaluationThis measurement is non-invasive, painless and is also carried out as part of the care in the follow-up of critical limb ischemia. It takes place like a blood pressure measurement except that it is carried out at the level of a toe. | Procedure or surgery | Prospective cohort |
| data collectionretrospective data | Other | Historical cohort |
Primary outcome
Toe pressure with Systolic pressure measurement device
Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
The Systolic pressure measurement device is suitable for the toes, as part of the diagnosis or monitoring of obliterating arteriopathy of the lower limbs, as for the fingers of the hand during assessments relating to arteriovenous fistulas. The Systolic pressure measurement device ingeniously uses photoplethysmography (PPG) associated with a unique algorithm developed and patented by Atys Medical. PPG makes it possible to detect, thanks to a photoelectric cell (sensor), variations in blood flow in skin traffic. The Systolic pressure measurement deviceputs the measurement of digital pressure pressure within the reach of all the stakeholders concerned (angiologists, nephrologists, diabetologists, vascular surgeons, wound and healing services, etc.).
6 secondary outcomes
Evaluation of Survival
Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of the absence of target lesion occlusion.
Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of target lesion revascularization
Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of major adverse limb events
Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation ofthe Wound healing with WiFi classification
Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
Evaluation of the Wound healing with colorimetry scale
Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12
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 10 Jun 2025.
- Individual participant dataSharing planned: Yes. The data is available from Pr DUACSSE. An email can be sent to her so that she can contact the data manager and owner, the Bordeaux University Hospital. The data can be made available after contractual agreement
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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.
Eric DUCASSE, MD, PhD principal investigator
University Hospital, Bordeaux
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing intensive toe pressure evaluation and data collection in people with Critical Limb Ischemia (CLI), run by University Hospital, Bordeaux at 1 site in France.
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 4 inclusion and 9 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 10 Jun 2025. 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 France. 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. Some participants in this study may receive a placebo. 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?
Contact Eric DUCASSE, MD, PhD (+335 56 79 55 25, eric.ducasse@chu-bordeaux.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Toe pressure with Systolic pressure measurement device (time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12). 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 10 Jun 2025.