NCT04308278Toboroz4. fázis
Study to Evaluate the Efficacy of 2LEBV® and 2LXFS® on Asthenia in Patients With an Epstein-Barr Virus Infection
Randomized, Placebo-controlled, Double Blind Study to Evaluate the Efficacy of 2LEBV® and 2LXFS® on Asthenia in Patients With an Epstein-Barr Virus Infection.
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. aug. 31.
Rövid összefoglaló (regiszter, angolul)
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.
- Állapot (regiszter)
- Toboroz
- Fázis (regiszter)
- 4. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 88 (tervezett)
- Első benyújtás
- 2020. márc. 11.
- Kezdés
- 2021. jan. 22.
- Elsődleges befejezés
- 2028. aug. 22.
- Fő szponzor
- Labo'Life
- NCT-szám
- NCT04308278
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 4. fázis
- Tervezett résztvevők: 88
- 2021. jan. 22. és az elsődleges befejezés (2028. aug. 22.) között
- 8 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
Ki nem vehet részt
Szó szerint a(z) ClinicalTrials.gov forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.
Korábbi kezelés
- Patient who have received any treatment with the 2LEBV® or 2LXFS®,
- Patients who have received any homeopathic treatment in the previous 2 months prior to the study,
- Patients having received immunotherapy or micro-immunotherapy during the last 3 months,
- Patients who participated in a clinical study in the previous 2-months period,
- Patients addicted to or using recreational drugs,
Más betegség
- Patient undergoing treatment for psychiatric disorders,
- Patients with severe immunodeficiency disease requiring long term treatment (*) or patients under chemotherapy or radiotherapy,
- Patient under guardianship and/or curatorship, (*) important renal or respiratory insufficiency, transplanted or grafted patients, HIV/AIDS, terminal cancer.
Egyéb
- Patients under immunosuppressive treatment,
- Patients with known lactose intolerance,
- Pregnant or breastfeeding women,
- Patients (and/or parents of patients if necessary) who are not sufficiently motivated to engage on the total study follow-up period, or likely to travel or to move before the end of the study,
- Patients under homeopathic or phytotherapy treatment,
Kiket keres a vizsgálat
- Patient who have a positive serology for EBV (IgG and/or IgM positive).
A regiszterben nem jelölt feltételek
- Pre-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-lasting exhaustion 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 deficit disorders, 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 the study during the pre-inclusion visit,
- Patients (and/or parents if necessary) having the faculties to understand and respect the constraints of the study,
- Signature of the Informed Consent Form by the patient (and/or parents if necessary).
Életkor a regiszterben: 12 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (8)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Private Practice | Aartselaar | Belgium | Toboroz |
| Private Practice | Brussels | Belgium | Toboroz |
| Private Practice | Ghent | Belgium | Toboroz |
| Private practice of Dr Pieterjan DEBBAUT | Heule | Belgium | Fut, nem toboroz |
| Private practice | Marche-en-Famenne | Belgium | Toboroz |
| Cabinet privé | Schoten | Belgium | Toboroz |
| Private practice | Stavelot | Belgium | Toboroz |
| Private practice | Waregem | Belgium | Toboroz |
Ez az oldal tájékoztatás, nem orvosi tanács. Bármely vizsgálatról az orvosoddal beszélj.