Chronic Ulcer of Leg or FootMATHCOWNCT05170984
MAtrix Therapy for Hard-to-heal ChrOnic Wounds
A study testing CACIPLIQ20® in people with Chronic Ulcer of Leg or Foot and Diabetic Foot Ulcer, run by Organ, Tissue, Regeneration, Repair and Replacement at 1 site in France.
Trial summary
CACIPLIQ20® is currently a class III CE marked medical device available in various European and non-European countries, and currently primarily used in managing hard-to-heal wounds. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Ulcer of Leg or Foot, Diabetic Foot Ulcer, Arterial Ulcer
- What is being tested?
- CACIPLIQ20®
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 191 participants
- Where
- 1 siteFrance
- Study dates
- 10 Feb 2022to 30 Dec 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
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
None listed.
Who cannot join
- Female patients who are pregnant, or lactating.
- Bedridden patients unable to spend at least one hour per day sitting in a chair.
- Patients suffering from severe cognitive problems precluding any voluntary participation to the study.
- Patients with, according to investigator's opinion, a very poor life expectancy.
- Patients with leg or foot ulcerations which are not of venous, arterial or diabetic origin (e.g. Martell's ulcer and related ulcers, pressure ulcers, traumatic wounds or burns)
- Patients whose target wound is located on an amputation stump.
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- Patients presenting with a fungating wound at the time of inclusion.
- Patients in an emergency situation and unable to give consent.
- Patients intolerant to one of the study device components or to heparinoids.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Prospective Cohort Survey of Foot and Leg Chronic Wounds Followed up to 20 Weeks After Initiation of CACIPLIQ20® add-on to Optimal Local Care
CACIPLIQ20® is currently a class III CE marked medical device available in various European and non-European countries, and currently primarily used in managing hard-to-heal wounds.
This study is a prospective and standardized recording of patients' data followed in real-life conditions to appreciate the benefits of a therapeutic strategy including CACIPLIQ20® use. It also aims at collecting data to follow-up the device's efficacy and safety and estimate its cost-effectiveness.
Read the detailed description
§ Study context:
CACIPLIQ20® is a bioengineered structural analogue of heparan sulfate glycosaminoglycans. Numerous experimental studies have provided strong evidence that CACIPLIQ20® promotes tissue regeneration by reconstructing the cellular microenvironment following tissue injury. Case studies collected in various clinical settings support the clinical interest of CACIPLIQ20® in the management of hard-to-heal chronic wounds.
CACIPLIQ20® is currently a class III CE marked medical device (NSAI-0050 CE MARK ECDEC-NL-A4) with the following indications:
Chronic ulcers showing no tendency to heal after 6 months of standard care, or still unhealed after 12 months, such as:
- Pressure ulcers;
- Peripheral arterial disease (such as Stage IV Leriche \& Fontaine) ulcers;
- Diabetic ulcers (including amputation).
CACIPLIQ20® is available in various European and non-European countries and currently primarily used in managing hard-to-heal wounds.
Therefore, there is an opportunity to organize a prospective and standardized recording of patients' data followed in real-life conditions to appreciate the benefits of a therapeutic strategy including CACIPLIQ20® use and to collect data that may help to highlight its efficacy and safety and estimate its cost-effectiveness.
§ Hard-to-heal leg/foot ulcerations:
Leg ulcers of venous, mixed or arterial origin as well as neuropathic or neuroischaemic diabetic foot ulcers represent the most prevalent chronic wounds followed and managed in daily practices.
Arterial leg ulcers and Diabetic foot ulcers (DFU)s (especially for neuroischaemic DFUs) have frequently a rather poor healing prognosis despite revascularization attempts and application of best local cares including, for DFUs, wearing of appropriate off-loading devices. The risk of deciding minor or major lower limb amputation is high and the chance to obtain wound closure at 20-24 weeks is, at the best, around 20-30%.
For leg ulcers of venous origin (ankle brachial pressure index (ABPI) ≥0.8) or of mixed origin (ABPI ranges between 0.6 and 0.8), the healing prognosis is better with application of best local cares and the use when the ABPI is >0.7 or 0.8 of an efficient venous bandaging. Nevertheless, when initiating the management of large old wounds (area >10 cm² and ulcer present for at least 6 months) the chance to obtain wound closure at 20-24 weeks is of 20-30% at best.
This survey will specifically include patients presenting a hard-to-heal foot/leg ulceration such as: leg ulcers of predominantly venous origin but with an ulcer surface >10 cm² and/or an estimated wound duration of at least 5 months, leg ulcer with arterial participation including critical limb ischemia, or neuropathic and neuroischaemic DFUs.
§ Study organization:
The inclusion of patients is decided the day when the addition of CACIPLIQ20® to the standard of local care is decided. The follow-up of the patient in the cohort will be carried out until the target wound is closed or up to a maximum of 20 weeks.
The inclusion and follow-up of patients are ensured, in agreement and in cooperation with the healthcare team of the subject, by doctors and expert nurses from the Cicat Occitanie network. This network relies on secured and validated teleconsultation tools. The inclusion of a patient in the cohort will not change the usual functioning of the network.
- Being tested
- CACIPLIQ20®
- Keywords
- CACIPLIQ20, Chronic Wound, Chronic Ulcer, Hard-to-heal Wound
- Medical subject headings
- Diabetic Foot, Varicose Ulcer
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
CACIPLIQ20®Device
Application of CACIPLIQ20® by spray, directly on the wound surface, after wound cleaning and debridement, twice a week, until wound closure (or up to 20 weeks maximum).
| Study group | Role | What they receive |
|---|---|---|
| CACIPLIQ20® | Experimental | Treatment of the target wound with CACIPLIQ20® in addition to optimal local care Receives: Device: CACIPLIQ20® |
What is being measured
The primary outcome is the main question the study is designed to answer.
Rate of wound closure
Wound closure defined as a 100% re-epithelialization, including:
- A confirmed complete closure (CCC), defined as a wound closure notified by investigator and confirmed by an independent reviewer when analysing wound photos.
- A possible complete closure (PCC), defined as a wound closure notified by investigator without confirmation by the independent reviewer (either no photo or photo of too poor quality or no unambiguous confirmation).
The primary endpoint is the sum of CCC and PCC.
Measured: Within 20 weeks after treatment initiation
Secondary outcomes (5)
Rate of adverse events (AEs) related to CACIPLIQ20® use
Rate of adverse events (AEs) occurring during the study course including serious and non-serious AEs, anticipated or unanticipated AEs, related to CACIPLIQ20® use, according to investigators' opinion.
Measured: From baseline to wound closure or 20 weeks after treatment initiation
Rate of device deficiencies (DDs)
Rate of device deficiencies (DDs) occurring during the study course including anticipated or unanticipated DDs.
Measured: From baseline to wound closure or 20 weeks after treatment initiation
Rate of wound closure according to the type of closure (CCC, PCC) and according to the nature of the treated wounds (Venous Leg Ulcers, Arterial Ulcers and Diabetic Foot Ulcers).
Measured: Within 20 weeks after treatment initiation
Time to wound closure
Measured: Within 20 weeks after treatment initiation
Changes in the Pain Visual Analogic Scale
Pain Visual Analogic Scale from 0 (no pain) to 10 (unbearable pain)
Measured: From baseline to wound closure or 20 weeks after treatment initiation
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Dec 2021
- Study start10 Feb 2022
- Primary completion1 Jul 2024
- Study completion30 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Ulcer of Leg or FootStudies 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
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 191 participants (actual)
Sponsor and investigators
- Lead sponsor
- Organ, Tissue, Regeneration, Repair and Replacement
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Luc TEOT, MD, PhD, Principal investigator, Réseau Cicat-Occitanie
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05170984
- Sponsor's protocol ID
- 2021-A01910-41
- Acronym
- MATHCOW
- Status last verified
- Nov 2025
- First submitted
- 23 Nov 2021
- Last updated
- 13 Apr 2026
- Results posted
- No
- Data monitoring committee
- Yes
- 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 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective Cohort Survey of Foot and Leg Chronic Wounds Followed up to 20 Weeks After Initiation of CACIPLIQ20® add-on to Optimal Local Care
- ClinicalTrials.gov ID
- NCT05170984
- Acronym / sponsor ID
- MATHCOW / 2021-A01910-41
- Keywords
- CACIPLIQ20, Chronic Wound, Chronic Ulcer, Hard-to-heal Wound
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 191 participants (actual)
- Lead sponsor
- Organ, Tissue, Regeneration, Repair and ReplacementIndustry (pharma, biotech, devices)
- Study start
- 10 Feb 2022 (actual)
- Primary completion
- 1 Jul 2024 (actual)
- Study completion
- 30 Dec 2024 (actual)
- First posted
- 28 Dec 2021 (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.
CACIPLIQ20® is currently a class III CE marked medical device available in various European and non-European countries, and currently primarily used in managing hard-to-heal wounds.
This study is a prospective and standardized recording of patients' data followed in real-life conditions to appreciate the benefits of a therapeutic strategy including CACIPLIQ20® use. It also aims at collecting data to follow-up the device's efficacy and safety and estimate its cost-effectiveness.
Detailed description
§ Study context:
CACIPLIQ20® is a bioengineered structural analogue of heparan sulfate glycosaminoglycans. Numerous experimental studies have provided strong evidence that CACIPLIQ20® promotes tissue regeneration by reconstructing the cellular microenvironment following tissue injury. Case studies collected in various clinical settings support the clinical interest of CACIPLIQ20® in the management of hard-to-heal chronic wounds.
CACIPLIQ20® is currently a class III CE marked medical device (NSAI-0050 CE MARK ECDEC-NL-A4) with the following indications:
Chronic ulcers showing no tendency to heal after 6 months of standard care, or still unhealed after 12 months, such as:
- Pressure ulcers;
- Peripheral arterial disease (such as Stage IV Leriche \& Fontaine) ulcers;
- Diabetic ulcers (including amputation).
CACIPLIQ20® is available in various European and non-European countries and currently primarily used in managing hard-to-heal wounds.
Therefore, there is an opportunity to organize a prospective and standardized recording of patients' data followed in real-life conditions to appreciate the benefits of a therapeutic strategy including CACIPLIQ20® use and to collect data that may help to highlight its efficacy and safety and estimate its cost-effectiveness.
§ Hard-to-heal leg/foot ulcerations:
Leg ulcers of venous, mixed or arterial origin as well as neuropathic or neuroischaemic diabetic foot ulcers represent the most prevalent chronic wounds followed and managed in daily practices.
Arterial leg ulcers and Diabetic foot ulcers (DFU)s (especially for neuroischaemic DFUs) have frequently a rather poor healing prognosis despite revascularization attempts and application of best local cares including, for DFUs, wearing of appropriate off-loading devices. The risk of deciding minor or major lower limb amputation is high and the chance to obtain wound closure at 20-24 weeks is, at the best, around 20-30%.
For leg ulcers of venous origin (ankle brachial pressure index (ABPI) ≥0.8) or of mixed origin (ABPI ranges between 0.6 and 0.8), the healing prognosis is better with application of best local cares and the use when the ABPI is >0.7 or 0.8 of an efficient venous bandaging. Nevertheless, when initiating the management of large old wounds (area >10 cm² and ulcer present for at least 6 months) the chance to obtain wound closure at 20-24 weeks is of 20-30% at best.
This survey will specifically include patients presenting a hard-to-heal foot/leg ulceration such as: leg ulcers of predominantly venous origin but with an ulcer surface >10 cm² and/or an estimated wound duration of at least 5 months, leg ulcer with arterial participation including critical limb ischemia, or neuropathic and neuroischaemic DFUs.
§ Study organization:
The inclusion of patients is decided the day when the addition of CACIPLIQ20® to the standard of local care is decided. The follow-up of the patient in the cohort will be carried out until the target wound is closed or up to a maximum of 20 weeks.
The inclusion and follow-up of patients are ensured, in agreement and in cooperation with the healthcare team of the subject, by doctors and expert nurses from the Cicat Occitanie network. This network relies on secured and validated teleconsultation tools. The inclusion of a patient in the cohort will not change the usual functioning of the network.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| CACIPLIQ20® | Experimental | Device: CACIPLIQ20®Treatment of the target wound with CACIPLIQ20® in addition to optimal local care |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (0 listed)
Key exclusion criteria (9 listed)
- Female patients who are pregnant, or lactating.
- Bedridden patients unable to spend at least one hour per day sitting in a chair.
- Patients suffering from severe cognitive problems precluding any voluntary participation to the study.
- Patients with, according to investigator's opinion, a very poor life expectancy.
- Patients with leg or foot ulcerations which are not of venous, arterial or diabetic origin (e.g. Martell's ulcer and related ulcers, pressure ulcers, traumatic wounds or burns)
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 |
|---|---|---|
| CACIPLIQ20®Application of CACIPLIQ20® by spray, directly on the wound surface, after wound cleaning and debridement, twice a week, until wound closure (or up to 20 weeks maximum). | Device | CACIPLIQ20® |
Primary outcome
Rate of wound closure
Time frame: Within 20 weeks after treatment initiation
Wound closure defined as a 100% re-epithelialization, including: * A confirmed complete closure (CCC), defined as a wound closure notified by investigator and confirmed by an independent reviewer when analysing wound photos. * A possible complete closure (PCC), defined as a wound closure notified by investigator without confirmation by the independent reviewer (either no photo or photo of too poor quality or no unambiguous confirmation). The primary endpoint is the sum of CCC and PCC.
5 secondary outcomes
Rate of adverse events (AEs) related to CACIPLIQ20® use
Time frame: From baseline to wound closure or 20 weeks after treatment initiation
Rate of device deficiencies (DDs)
Time frame: From baseline to wound closure or 20 weeks after treatment initiation
Rate of wound closure according to the type of closure (CCC, PCC) and according to the nature of the treated wounds (Venous Leg Ulcers, Arterial Ulcers and Diabetic Foot Ulcers).
Time frame: Within 20 weeks after treatment initiation
Time to wound closure
Time frame: Within 20 weeks after treatment initiation
Changes in the Pain Visual Analogic Scale
Time frame: From baseline to wound closure or 20 weeks after treatment initiation
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Apr 2026.
- Individual participant dataSharing planned: No
Related trials for Chronic Ulcer of Leg or Foot
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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.
Luc TEOT, MD, PhD principal investigator
Réseau Cicat-Occitanie
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing CACIPLIQ20® in people with Chronic Ulcer of Leg or Foot and Diabetic Foot Ulcer, run by Organ, Tissue, Regeneration, Repair and Replacement 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 0 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: finished, as of the sponsor's last update on 13 Apr 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 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. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Rate of wound closure (time frame: Within 20 weeks after treatment initiation). 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 Apr 2026; AzTrials last refreshed its copy on 6 Nov 2026.