NCT07326033RecruitingPhase 2
Efficacy and safety of allogenic cultured Adipose-derived mesenchymal stromal cell injections on MoUth fibrosis and handicap in patients with Systemic sclEroderma
Source: EU CTIS (euclinicaltrials.eu) · Last updated 1 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
To assess efficacy of allogenic cultured adipose-derived stromal cell injections on orofacial fibrosis and handicap at week 12 in patients with systemic scleroderma, as measured by the MHISS scale.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- First submitted
- 16 May 2025
- Start date
- 13 Oct 2026
- Lead sponsor
- Centre Hospitalier Universitaire De Toulouse
- Diseases
- Systemic sclerosis (scleroderma)
- EU CT number
- 2024-518516-39-00
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 50
- 5 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.
Who cannot take part
Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patient participating in a clinical trial or having participated in a clinical trial within the previous 3 months,
- Injection of botulinum toxin within 4 weeks prior to "inclusion visit",
- Patient who underwent autologous hematopoietic stem cell transplantation (HSCT) within less than 1 year,
- Local active labial herpes virus within 1 week prior to "inclusion visit",
- Radio- or chemotherapy in progress,
Other illness
- History of cancer in the last five years, except for successfully excised basal cell/squamous cell carcinoma, or successfully excised early melanoma of the skin. Subjects, who had a successful tumor resection or radiation or chemotherapy more than 5 years prior to inclusion and no recurrence, may be enrolled in the study,
- Vulnerable patient (persons deprived of their liberty by judicial or administrative decision, persons undergoing psychiatric treatment, persons admitted to a health or social establishment for purposes other than research) according to article L1121-6 of the Public Health Code
Other
- Patients with an indication for intensification by autologous HSCT (according to EBMT guidelines and national MATHEC-SFGMTC guidelines),
- Females who are pregnant or breastfeeding or plan to be or do so during the course of this study,
- Women of childbearing potential (WOCBP) who are sexually active and unwilling to use an adequate birth control method,
Who the study is looking for
- Male or female patient ≥18 years of age,
- Patient with systemic scleroderma according to the 2013 ACR/EULAR classification criteria,
- Mouth Handicap in Systemic Sclerosis Scale (MHISS) score more than or equal to 20 (0-48),
- Rodnan skin score on the face more than or equal to 1,
- Maximal mouth opening of less than 40 mm (distance between the dental arches)
- Patient must have provided written informed consent prior to enrolment,
- Patient must be able to understand their requirements of participating in the protocol.
- Patient affiliated to a social security system.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (5)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Centre hospitalier Universitaire de Bordeaux Coordinator of this site? Confirm its status | Bordeaux | France | Recruiting |
| Centre Hospitalier Universitaire de Dijon Coordinator of this site? Confirm its status | Dijon | France | Recruiting |
| Centre Hospitalier Universitaire De Montpellier Coordinator of this site? Confirm its status | Montpellier Cedex 5 | France | Recruiting |
| Centre Hospitalier Universitaire de Nantes Coordinator of this site? Confirm its status | Nantes | France | Recruiting |
| Centre Hospitalier Universitaire De Toulouse Coordinator of this site? Confirm its status | Toulouse Cedex 9 | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.