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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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
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.

France1 site
  • Réseau Cicat-Occitanie

    Montpellier, 34295

Other trials in France

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 groups in NCT05170984
Study groupRoleWhat they receive
CACIPLIQ20®ExperimentalTreatment 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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. Time to wound closure

    Measured: Within 20 weeks after treatment initiation

  5. 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.

  1. First posted28 Dec 2021
  2. Study start10 Feb 2022
  3. Primary completion1 Jul 2024
  4. Study completion30 Dec 2024

Resources

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)
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

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.

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