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NCT Number: NCT07549594

Prophylaxis of Recurrent Erysipelas in Lower Limbs: compreSsion thErapy vs aNTibiotics and Compression Therapy.

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

AMIENS, Amiens, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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)
  • 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

Exclusion criteria

  • 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)
  • 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.

Treatment and study plan

Elastic stockings

Device

thighs-high stockings, produced by means of circular knitting, corresponding to the patient's measurements

Phenoxymethylpenicillin

Drug

Phenoxymethylpenicillin (Oracilline) 1 Million UI twice a day, per os, during one year

Primary outcomes

  1. 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

Secondary outcomes

  1. 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

  2. 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

    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.

  3. Severity of recurrence: presence of skin necrosis or ulceration

    Time frame: From enrollment to the end of treatment at 12 months

  4. Assessment of adverse effects and serious adverse effects during the study

    Time frame: From enrollment to the end of treatment at 12 months

  5. 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

    Stantardized questionnaire with minimum value = 0 (better out come) and maximum value = 30 (worse outcome)

  6. 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

    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.

  7. Adherence: number of days per week that compression was worn

    Time frame: From enrollment to the end of treatment at 12 months

    Using a patient diary. Patients' adherence with compression therapy, which is known to be low

  8. Adherence: assessment of oedema by circumferential measurements

    Time frame: Month 0, Month 6, Month 12

    By evaluator (assessor-blinded during the follow-up) and devoted tool (excel calculator) will be built accordingly to give automatically the truncated cone formula

  9. Adherence: number of days per week that antibiotics is taken

    Time frame: From enrollment to the end of treatment at 12 months

    Using a patient diary

Study contacts

Contact information is provided by the study sponsor or research team.

Loïc VAILLANT

CONTACT

[email protected]

0247479080

Sponsors and collaborators

Lead sponsor

University Hospital, Tours

Other

Registry information

Official study title

Prophylaxis of Recurrent Erysipelas in Lower Limbs: compreSsion thErapy vs aNTibiotics and Compression Therapy. A Non-inferiority, Multicentre, Randomized Clinical Trial.

Acronym: PRESENT

Important dates

Study start
2026
Primary completion
2030
Study completion
2030
First posted
Apr 24, 2026
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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