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

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Tours

About this 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.

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Already wore effective compression therapy (worn at least 5 days a week) in the 3 months before randomization

Trial design

Design model

Parallel

Treatments tested in this trial

  • 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

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Experimental arm : supervised compression therapy + emollient cream during 12 monthsExperimental treatment 1 intervention
Group B: Control group: supervised compression therapy + emollient cream + oral penicillin (phénoxyméthylpéActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

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

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

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)

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.

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

Other outcomes

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