Study to Evaluate the Efficacy of 2LEBV® and 2LXFS® on Asthenia in Patients With an Epstein-Barr Virus Infection

Last updated: October 29, 2024
Sponsor: Labo'Life
Overall Status: Active - Recruiting

Phase

4

Condition

N/A

Treatment

2LEBV® / 2LXFS®

Placebo

Clinical Study ID

NCT04308278
LLB-2019-03
  • Ages > 12
  • All Genders

Study Summary

Worldwide, 95% of adults are infected with Epstein-Barr Virus (EBV). These infections may cause different diseases. In most cases, EBV infection is asymptomatic because of a highly effective host immune response. Some individuals develop infectious mononucleosis (a self-limiting lymphoproliferative disorder in adolescents and young adults that is considered to be the primary infection), while others develop chronic fatigue syndrome, EBV-associated lymphoid, or epithelial malignancies.

Today, there is no available treatment to treat and destroy EBV. The treatment is essentially symptomatic (treatment of the symptoms and not of the virus itself) with analgesics for pain for example.

The studied drugs are 2LEBV® and 2LXFS®, from Labo'Life company, and the treatment schema is the same for the two drugs: it consists in taking the content of one capsule per day, sequentially, according to capsules' numerical order: 1 through 10. When capsule number 10 is taken, capsule 1 of the next blister should be taken on the next day to continue the treatment.

The duration of treatment will be of 6 months of continuous intake of the content of 1 capsule/day.

The aim of this study is to provide additional information on effectiveness on the 2LEBV® and 2LXFS®in the treatment of EBV chronic and acute infections, and in particular to demonstrate their effectiveness versus placebo in the reduction of asthenia and other symptoms in EBV infection.

Eligibility Criteria

Inclusion

Pré-Inclusion Criteria:

  • Patients, male or female, aged 12 years and older,

  • Patient with fatigue for 1 month or more,

  • Patient with at least two other symptoms among the following: Long-lastingexhaustion even after light exertion, subfebrile state, fever, loss of appetite,nausea, angina, conjunctivis, sensitive cervical or axillary lymph nodes,erythematous and swollen tonsil, headaches, sore throat, myalgia, muscular weakness,arthralgia, splenomegaly, visual disorders, memory disorders, attention deficitdisorders, sleep disorders, gastrointestinal disorders, breathing disorders,cardiovascular disorders.

  • Patient (and/or parents if necessary) agrees to perform serology for the study,

  • Patient (and/or parents if necessary) agrees to perform lymphocyte typing for thestudy during the pre-inclusion visit,

  • Patients (and/or parents if necessary) having the faculties to understand andrespect the constraints of the study,

  • Signature of the Informed Consent Form by the patient (and/or parents if necessary).

Inclusion Criteria:

  • Patient who have a positive serology for EBV (IgG and/or IgM positive).

Exclusion

Exclusion Criteria:

  • Patient who have received any treatment with the 2LEBV® or 2LXFS®,

  • Patients who have received any homeopathic treatment in the previous 2 months priorto the study,

  • Patients under immunosuppressive treatment,

  • Patient undergoing treatment for psychiatric disorders,

  • Patients having received immunotherapy or micro-immunotherapy during the last 3months,

  • Patients with known lactose intolerance,

  • Pregnant or breastfeeding women,

  • Patients who participated in a clinical study in the previous 2-months period,

  • Patients (and/or parents of patients if necessary) who are not sufficientlymotivated to engage on the total study follow-up period, or likely to travel or tomove before the end of the study,

  • Patients with severe immunodeficiency disease requiring long term treatment (*) orpatients under chemotherapy or radiotherapy,

  • Patients under homeopathic or phytotherapy treatment,

  • Patients addicted to or using recreational drugs,

  • Patient under guardianship and/or curatorship, (*) important renal or respiratoryinsufficiency, transplanted or grafted patients, HIV/AIDS, terminal cancer.

Study Design

Total Participants: 88
Treatment Group(s): 2
Primary Treatment: 2LEBV® / 2LXFS®
Phase: 4
Study Start date:
January 22, 2021
Estimated Completion Date:
August 30, 2026

Connect with a study center

  • Private Practice

    Aartselaar, 2630
    Belgium

    Active - Recruiting

  • Private Practice

    Boortmeerbeek, 3190
    Belgium

    Terminated

  • Private Practice

    Brussels, 1040
    Belgium

    Active - Recruiting

  • Private practice

    Brussels, 1040
    Belgium

    Active - Recruiting

  • Private Practice

    Bruxelles, 1200
    Belgium

    Active - Recruiting

  • Private Practice

    Gent, 9000
    Belgium

    Active - Recruiting

  • Private Practice

    Jette, 1090
    Belgium

    Site Not Available

  • Private Practice

    Limal, 1300
    Belgium

    Site Not Available

  • Private practice

    Marche-en-Famenne, 6900
    Belgium

    Active - Recruiting

  • Private Practice

    Nivelles, 1400
    Belgium

    Site Not Available

  • Cabinet privé

    Schoten, 2900
    Belgium

    Active - Recruiting

  • Private practice

    Stavelot, 4790
    Belgium

    Active - Recruiting

  • Private practice

    Waregem, 8790
    Belgium

    Active - Recruiting

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