Recurrent ErysipelasPhase 4PRESENTNCT07549594
Prophylaxis of Recurrent Erysipelas in Lower Limbs: compreSsion thErapy vs aNTibiotics and Compression Therapy.
A Phase 4 study testing elastic stockings and Phenoxymethylpenicillin in people with Recurrent Erysipelas, run by University Hospital, Tours at 25 sites in France.
Trial summary
Erysipelas (superficial cellulitis) is a frequent streptococcal bacterial infection. Each episode of erysipelas may worsen preexisting lymphedema and evolve to life-threatening necrotizing soft-tissue infection. Moreover, each attack of cellulitis may worsen lymphatic damage and therefore favour additional attacks. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Recurrent Erysipelas
- What is being tested?
- elastic stockings and Phenoxymethylpenicillin
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- 25 sitesFrance
- Study dates
- 1 Apr 2026to 1 Apr 2030
- Phase
- Phase 4
- 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
- Male or female
- ≥ 18 years of age
- At least 2 episodes of recurrent erysipelas at the same leg within the previous 52 weeks, and no more than five episodes of erysipelas in the same areas of the lower limbs during the year before randomization
- The last recurrent erysipelas have to be diagnosed within the previous 3 months
- BMI < 40 kg/m2 (no morbid obesity)
- Able to apply the compression alone or with a helper (e.g., nurse, household member)
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- Affiliated with a social security regimen
- Able to consent and written informed consent obtained from the participant
- Able to understand the aims of the study and to comply with the requirements of the study
- Able to participate and be followed up during the study period
Who cannot join
- Any causes of immunosuppression: known HIV+ infection, organ transplantation, bonemarrow transplantation, immunosuppressive regimens for any disease, malignancy or lymphoproliferative disorder
- Receiving antibiotic treatment for erysipelas
- Received antibiotic prophylaxis for recurrent erysipelas in the year before randomization
- Received short- or long-term antibiotic therapy for a condition other than erysipelas
- Already wore effective compression therapy (worn at least 5 days a week) in the 3 months before randomization
- Contraindication to compression therapy (ie heart failure, arterial occlusive disease,including obliterative peripheral arterial disease with a systolic pressure index < 0.6, advanced diabetic microangiopathy for compression > 30 mmHg, phlegmasia cerulea dolens, and septic thrombosis)
Show all 14Show fewer
- History of known hypersensitivity to beta-lactamines or contraindications to Phenoxymethylpenicillin (Oracilline) or to any of the other components of the medicine as per its SmPC
- Contraindications to the emollient cream in accordance with its SmPC
- Diabetic foot and fractures
- Woman of childbearing potential not using a highly effective method of contraception*, or having a desire to conceive, during the whole trial duration. A β-HCG test will be performed in all woman of childbearing potential
- Persons covered by articles L1121-5 to L1121-8 of the Code de Santé Publique (corresponding to all protected persons: pregnant women, parturients, nursing mothers, persons deprived of their liberty by judicial or administrative decision, minors, and persons subject to a legal protection measure: guardianship or trusteeship).
- Participation in another interventional research with an investigational drug or medical device.
- Mental state rendering the person giving consent incapable of understanding the trial;
- Patient being the investigator, or any member of the team or relative of the investigator directly involved in the trial, including assistant doctors, pharmacists, nurses, trial coordinator.
Trial locations and contacts
25 sites in 1 country. Contact the study team or a site near you to ask about taking part.
25 sites in 1 country
France25 sites
AMIENS
Amiens
Guillaume CHABY, 03 22 45 58 43, Chaby.Guillaume@chu-amiens.fr
Bordeaux-D
Bordeaux
Marie BEYLOT-BARRY, 05 57 82 25 09, marie.beylot-barry@chu-bordeaux.fr
Bordeaux-I
Bordeaux
Charles CAZANAVE, 05 57 82 11 03, charles.cazanave@chu-bordeaux.fr
TOURS-D
Chambray-lès-Tours
Valérie TAUVERON, 0247472409, v.tauveron@chu-tours.fr
CRETEIL
Créteil
Camille HUA, 06 88 33 97 09, Camille.hua@aphp.fr
DIJON
Dijon
Lionel PIROTH, 03 80 29 52 40, lionel.piroth@chu-dijon.fr
GRENOBLE
La Tronche
Sophie BLAISE, 04 76 76 55 47, sblaise@chu-grenoble.fr
LE MANS
Le Mans
Hervé MAILLARD, 02 43 43 24 85, hmaillard@ch-lemans.fr
Lille Ghicl
Lille
Philippe MODIANO, 0359208776, modiano.philippe@ghicl.net
LYON
Lyon
Sarah SOUEGES, 0472071274, sarah.soueges@chu-lyon.fr
NANTES-D
Nantes
Gaëlle QUEREUX, 0240083144, gaelle.quereux@chu-nantes.fr
NANTES-I
Nantes
David BOUTOILLE, 0240083391, david.boutoille@chu-nantes.fr
ORLEANS
Orléans
Antoine MARCHAND, 02 38 57 50 37, antoine.marchand@chu-orleans.fr
Paris Cognacq-Jay
Paris
VIGNES, 0145308090, stephane.vignes@cognacq-jay.fr
Paris La Pitie
Paris
Gentiane MONSEL, 0184827371, gentiane.monsel@aphp.fr
Paris St Louis-I
Paris
Jean-Michel MOLINA, 0142499066, jean-michel.molina@aphp.fr
Paris St-Antoine-I
Paris
Laure SURGERS, 0249280939, Laure.surgers@aphp.fr
POITIERS
Poitiers
Ewa HAINAUT, 0549443964, Ewa.hainaut@chu-poitiers.fr
REIMS
Reims
Maxime HENTZIEN, 0326787189, mhentzien@chu-reims.fr
RENNES-D
Rennes
Florence POIZEAU, 0299284321, Florence.POIZEAU@chu-rennes.fr
ROUEN
Rouen
Priscille CARVALHO, 0232886841, Priscille.Carvalho@chu-rouen.fr
St-Etienne
Saint-Etienne
Jean-Luc PERROT, 0477828508, j.luc.perrot@chu-st-etienne.fr
La Reunion
Saint-Pierre
Antoine BERTOLOTTI, 0262359191, antoine.bertolotti@chu-reunion.fr
Strasbourg
Strasbourg
Cédric LENORMAND, 0388115119, cedric.lenormand@chru-strasbourg.fr
TOURS-I
Tours
Adrien LEMAIGNEN, 0218370644, adrien.lemaignen@univ-tours.fr
About this study
Official title: Prophylaxis of Recurrent Erysipelas in Lower Limbs: compreSsion thErapy vs aNTibiotics and Compression Therapy. A Non-inferiority, Multicentre, Randomized Clinical Trial.
Erysipelas (superficial cellulitis) is a frequent streptococcal bacterial infection. Each episode of erysipelas may worsen preexisting lymphedema and evolve to life-threatening necrotizing soft-tissue infection. Moreover, each attack of cellulitis may worsen lymphatic damage and therefore favour additional attacks. Recurrence is frequent: 10-30% of cases and even up to 50%. In this context, at least 2 episodes of erysipelas in the same limb during a 1-year period defines recurrent erysipelas requiring prophylaxis. Such prophylaxis is based usually on penicillin therapy. Compression was evaluated only in a monocentric randomized controlled trial, and was never compared to antibioprophylaxis.
The investigators hypothesized that compression therapy alone might represent a single intervention for prophylaxis of erysipelas recurrence as efficient as long-term antibiotic prophylaxis with compression therapy combined.
Read more
This study is a multicenter, parallel groups, assessor-blinded, non-inferiority, randomized clinical trial. Main objective is to evaluate whether supervised compression therapy alone is non-inferior to supervised compression therapy + oral penicillin in controlling relapse of recurrent erysipelas. Secondary objectives are to assess time to first recurrence ; to assess the severity of the recurrence ; to assess the safety of the intervention to assess the quality of life during the prophylaxis phase ; to assess the adherence of patients with the intervention and to assess, in a joint analysis, that supervised compression therapy is both not inferior in terms of QALY and not more expensive at 1 year than supervised compression therapy + antibiotic.
The study will included male or female adults who have had at least 2 episodes of recurrent erysipelas at the same leg within the previous 52 weeks, and no more than five episodes of erysipelas in the same areas of the lower limbs during the year before randomization. Experimental group is supervised compression therapy + emollient cream during 12 months and control group is supervised compression therapy + emollient cream + oral penicillin (phénoxyméthylpénicilline) during 12 months Main outcome is the proportion of patients with at least one recurrence of erysipelas during the 1-year prophylaxis phase, performed by an assessor-blinded.
Patients will be identified in a hospital setting, or referred by physicians servicing the local region, or by direct advertising through patients' associations. If the patient gives consent to participate, at the end of a inclusion visit (V0), the randomization will be performed via the e-CRF. Prescriptions will then be issued on inclusion. Control group who will start antibiotic treatment at inclusion. A run-in period of 7 ±2 days will be planned between V0 and the beginning of the compression therapy for the both group, in order to get the prescribed elastic stockings, and to train the nurse in charge of the compression supervision. A nurse trained in the study will supervise the first applications of the compression in the patient's home. After inclusion visit (V0), a home visit by the liberal IDE will be planned at M1 for to check daily adherence (use of ATB or/and wearing compression and application of emollients). A patient diary must be completed from inclusion and during the follow-up period. Two telemedicine clinic were scheduled at M3 and M9 and two study visits were scheduled at M6 and M12 with a complete physical examination. All the evaluations will be performed by a blinded evaluator investigator. Supplementary telemedicine clinic(s) in case of potential recurrence of erysipelas will be done by the blinded evaluator in the presence of the nurse who will be at bedside of patient.
The organization and design of the study will be realistic, and thus is designed to facilitate its feasibility and generalizability of results. In case of demonstration of non-inferiority of supervised compression therapy, patients with recurrent erysipelas will be spared of antibiotics first-line, and therefore suppress the impact of both long-term antibiotics on gut microbiota individuals and health burden of antibiotics at the population level.
- Conditions
- Recurrent Erysipelas
- Being tested
- elastic stockings, Phenoxymethylpenicillin
- Keywords
- Supervised compression, Oral penicillin, Controlling relapse of erysipelas, Randomized non-inferiority clinical trial
- Medical subject headings
- Erysipelas
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
elastic stockingsDevice
thighs-high stockings, produced by means of circular knitting, corresponding to the patient's measurements
PhenoxymethylpenicillinDrug
Phenoxymethylpenicillin (Oracilline) 1 Million UI twice a day, per os, during one year
| Study group | Role | What they receive |
|---|---|---|
| Experimental arm : supervised compression therapy + emollient cream during 12 months | Experimental | Not described Receives: Device: elastic stockings |
| Control group: supervised compression therapy + emollient cream + oral penicillin (phénoxyméthylpé | Active comparator | Not described Receives: Device: elastic stockings; Drug: Phenoxymethylpenicillin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of patients with at least one recurrence of erysipelas during the 1-year prophylaxis phase, performed by a assessor-blinded
Proportion of patients with at least one recurrence of erysipelas during the 1-year prophylaxis phase, performed by a assessor-blinded Diagnosis will be done by a blinded evaluator (investigator) different from those who recruited the patients, in the following 48h after the first sign of recurrence (fever, chills and/or erythematous plaque).
Recurrence of erysipelas will be diagnosed as sudden onset (<24h) of a well demarcated cutaneous inflammation (redness, warmth, edema and pain), with fever (>38°C) and/or chills
Measured: From enrollment to the end of treatment at 12 months
Secondary outcomes (9)
Time to the first confirmed recurrence of erysipelas
Measured: From enrollment to the first confirmed recurrence of erysipelas, e.g.up to 52 weeks
Severity of recurrence : erysipelas-related hospital admission (number of nights in hospital for cellulitis)
Erysipelas-related hospital admission : number of nights in hospital for cellulitis because treatment of erysipelas is normally an outpatient treatment, hospital admission is considered as a marker of severity of erysipelas.
Measured: From enrollment to the end of treatment at 12 months
Severity of recurrence: presence of skin necrosis or ulceration
Measured: From enrollment to the end of treatment at 12 months
Assessment of adverse effects and serious adverse effects during the study
Measured: From enrollment to the end of treatment at 12 months
Quality of life: Dermatology Life Quality Index (DLQI)
Stantardized questionnaire with minimum value = 0 (better out come) and maximum value = 30 (worse outcome)
Measured: Month 0, Month 3, Month 6, Month 9, Month 12 and in case of potential recurrence, e.g.up to 52 weeks
Quality of life: EuroQuol-5 Dimensions-5 Levels standardised questionnaire (EQ-5D-5L)
EQ-5D-5L (EuroQuol 5 Dimensions 5 Levels standardised questionnaire) was introduced by the EuroQol Group in 2009 to improve the instrument's sensitivity and to reduce ceiling effects.
Measured: Month 0, Month 3, Month 6, Month 9, Month12 and in case of potential recurrence
Adherence: number of days per week that compression was worn
Using a patient diary. Patients' adherence with compression therapy, which is known to be low
Measured: From enrollment to the end of treatment at 12 months
Adherence: assessment of oedema by circumferential measurements
By evaluator (assessor-blinded during the follow-up) and devoted tool (excel calculator) will be built accordingly to give automatically the truncated cone formula
Measured: Month 0, Month 6, Month 12
Adherence: number of days per week that antibiotics is taken
Using a patient diary
Measured: From enrollment to the end of treatment at 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Apr 2026
- Study start1 Apr 2026 (estimated)
- Primary completion1 Apr 2030 (estimated)
- Study completion1 Apr 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Recurrent ErysipelasStudies of the same condition, open and under way.
- More trials run by University Hospital, ToursThe 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Tours
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07549594
- Sponsor's protocol ID
- DR230313
- Acronym
- PRESENT
- Status last verified
- Apr 2026
- First submitted
- 3 Apr 2026
- Last updated
- 24 Apr 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 24 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prophylaxis of Recurrent Erysipelas in Lower Limbs: compreSsion thErapy vs aNTibiotics and Compression Therapy. A Non-inferiority, Multicentre, Randomized Clinical Trial.
- ClinicalTrials.gov ID
- NCT07549594
- Acronym / sponsor ID
- PRESENT / DR230313
- Conditions
- Recurrent Erysipelas
- Keywords
- Supervised compression, Oral penicillin, Controlling relapse of erysipelas, Randomized non-inferiority clinical trial
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- University Hospital, ToursUniversity, hospital or other
- Study start
- 1 Apr 2026 (estimated)
- Primary completion
- 1 Apr 2030 (estimated)
- Study completion
- 1 Apr 2030 (estimated)
- First posted
- 24 Apr 2026 (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.
Erysipelas (superficial cellulitis) is a frequent streptococcal bacterial infection. Each episode of erysipelas may worsen preexisting lymphedema and evolve to life-threatening necrotizing soft-tissue infection. Moreover, each attack of cellulitis may worsen lymphatic damage and therefore favour additional attacks. Recurrence is frequent: 10-30% of cases and even up to 50%. In this context, at least 2 episodes of erysipelas in the same limb during a 1-year period defines recurrent erysipelas requiring prophylaxis. Such prophylaxis is based usually on penicillin therapy. Compression was evaluated only in a monocentric randomized controlled trial, and was never compared to antibioprophylaxis.
The investigators hypothesized that compression therapy alone might represent a single intervention for prophylaxis of erysipelas recurrence as efficient as long-term antibiotic prophylaxis with compression therapy combined.
This study is a multicenter, parallel groups, assessor-blinded, non-inferiority, randomized clinical trial. Main objective is to evaluate whether supervised compression therapy alone is non-inferior to supervised compression therapy + oral penicillin in controlling relapse of recurrent erysipelas. Secondary objectives are to assess time to first recurrence ; to assess the severity of the recurrence ; to assess the safety of the intervention to assess the quality of life during the prophylaxis phase ; to assess the adherence of patients with the intervention and to assess, in a joint analysis, that supervised compression therapy is both not inferior in terms of QALY and not more expensive at 1 year than supervised compression therapy + antibiotic.
The study will included male or female adults who have had at least 2 episodes of recurrent erysipelas at the same leg within the previous 52 weeks, and no more than five episodes of erysipelas in the same areas of the lower limbs during the year before randomization. Experimental group is supervised compression therapy + emollient cream during 12 months and control group is supervised compression therapy + emollient cream + oral penicillin (phénoxyméthylpénicilline) during 12 months Main outcome is the proportion of patients with at least one recurrence of erysipelas during the 1-year prophylaxis phase, performed by an assessor-blinded.
Patients will be identified in a hospital setting, or referred by physicians servicing the local region, or by direct advertising through patients' associations. If the patient gives consent to participate, at the end of a inclusion visit (V0), the randomization will be performed via the e-CRF. Prescriptions will then be issued on inclusion. Control group who will start antibiotic treatment at inclusion. A run-in period of 7 ±2 days will be planned between V0 and the beginning of the compression therapy for the both group, in order to get the prescribed elastic stockings, and to train the nurse in charge of the compression supervision. A nurse trained in the study will supervise the first applications of the compression in the patient's home. After inclusion visit (V0), a home visit by the liberal IDE will be planned at M1 for to check daily adherence (use of ATB or/and wearing compression and application of emollients). A patient diary must be completed from inclusion and during the follow-up period. Two telemedicine clinic were scheduled at M3 and M9 and two study visits were scheduled at M6 and M12 with a complete physical examination. All the evaluations will be performed by a blinded evaluator investigator. Supplementary telemedicine clinic(s) in case of potential recurrence of erysipelas will be done by the blinded evaluator in the presence of the nurse who will be at bedside of patient.
The organization and design of the study will be realistic, and thus is designed to facilitate its feasibility and generalizability of results. In case of demonstration of non-inferiority of supervised compression therapy, patients with recurrent erysipelas will be spared of antibiotics first-line, and therefore suppress the impact of both long-term antibiotics on gut microbiota individuals and health burden of antibiotics at the population level.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Experimental arm : supervised compression therapy + emollient cream during 12 months | Experimental | Device: elastic stockings |
| Control group: supervised compression therapy + emollient cream + oral penicillin (phénoxyméthylpé | Active comparator | Device: elastic stockings, Drug: Phenoxymethylpenicillin |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- Male or female
- ≥ 18 years of age
- At least 2 episodes of recurrent erysipelas at the same leg within the previous 52 weeks, and no more than five episodes of erysipelas in the same areas of the lower limbs during the year before randomization
- The last recurrent erysipelas have to be diagnosed within the previous 3 months
- BMI < 40 kg/m2 (no morbid obesity)
Key exclusion criteria (14 listed)
- Any causes of immunosuppression: known HIV+ infection, organ transplantation, bonemarrow transplantation, immunosuppressive regimens for any disease, malignancy or lymphoproliferative disorder
- Receiving antibiotic treatment for erysipelas
- Received antibiotic prophylaxis for recurrent erysipelas in the year before randomization
- Received short- or long-term antibiotic therapy for a condition other than erysipelas
- Already wore effective compression therapy (worn at least 5 days a week) in the 3 months before randomization
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 |
|---|---|---|
| elastic stockingsthighs-high stockings, produced by means of circular knitting, corresponding to the patient's measurements | Device | Control group: supervised compression therapy + emollient cream + oral penicillin (phénoxyméthylpé, Experimental arm : supervised compression therapy + emollient cream during 12 months |
| PhenoxymethylpenicillinPhenoxymethylpenicillin (Oracilline) 1 Million UI twice a day, per os, during one year | Drug | Control group: supervised compression therapy + emollient cream + oral penicillin (phénoxyméthylpé |
Primary outcome
Proportion of patients with at least one recurrence of erysipelas during the 1-year prophylaxis phase, performed by a assessor-blinded
Time frame: From enrollment to the end of treatment at 12 months
Proportion of patients with at least one recurrence of erysipelas during the 1-year prophylaxis phase, performed by a assessor-blinded Diagnosis will be done by a blinded evaluator (investigator) different from those who recruited the patients, in the following 48h after the first sign of recurrence (fever, chills and/or erythematous plaque). Recurrence of erysipelas will be diagnosed as sudden onset (<24h) of a well demarcated cutaneous inflammation (redness, warmth, edema and pain), with fever (>38°C) and/or chills
9 secondary outcomes
Time to the first confirmed recurrence of erysipelas
Time frame: From enrollment to the first confirmed recurrence of erysipelas, e.g.up to 52 weeks
Severity of recurrence : erysipelas-related hospital admission (number of nights in hospital for cellulitis)
Time frame: From enrollment to the end of treatment at 12 months
Severity of recurrence: presence of skin necrosis or ulceration
Time frame: From enrollment to the end of treatment at 12 months
Assessment of adverse effects and serious adverse effects during the study
Time frame: From enrollment to the end of treatment at 12 months
Quality of life: Dermatology Life Quality Index (DLQI)
Time frame: Month 0, Month 3, Month 6, Month 9, Month 12 and in case of potential recurrence, e.g.up to 52 weeks
Quality of life: EuroQuol-5 Dimensions-5 Levels standardised questionnaire (EQ-5D-5L)
Time frame: Month 0, Month 3, Month 6, Month 9, Month12 and in case of potential recurrence
Adherence: number of days per week that compression was worn
Time frame: From enrollment to the end of treatment at 12 months
Adherence: assessment of oedema by circumferential measurements
Time frame: Month 0, Month 6, Month 12
Adherence: number of days per week that antibiotics is taken
Time frame: From enrollment to the end of treatment at 12 months
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 24 Apr 2026.
- Individual participant dataSharing planned: Undecided
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.
25 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing elastic stockings and Phenoxymethylpenicillin in people with Recurrent Erysipelas, run by University Hospital, Tours at 25 sites 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 10 inclusion and 14 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 24 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 25 sites 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.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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 Loïc VAILLANT (0247479080, loic.vaillant@univ-tours.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Proportion of patients with at least one recurrence of erysipelas during the 1-year prophylaxis phase, performed by a assessor-blinded (time frame: From enrollment to the end of treatment at 12 months). 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 24 Apr 2026.