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NCT07015411Toboroz

Neuro-Complex & Multi Supplements for Migraine Prevention

Effectiveness of an Orally Administered and Combined Neuro-Complex & Multi Supplements in the Prevention of Migraine in Adult

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. jún. 11. · Több mint 12 hónapja nem frissült - kérdezd meg a helyszínt, nyitott-e még

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Rövid összefoglaló (regiszter, angolul)

The goal of this prospective, monocentric, open-label, non-randomized and single arm study is to evaluate a reduction of migraine days per months (MDM) by 25% by using the combined supplementation with Neuro-Complex \& Multi after 8 weeks of product intake on participants with diagnosis of migraine meeting the criteria of the International Classification of Headache Disorders (ICHD-3) (with or without aura). The main endpoint of this clinical trial is : The mean changes in migraine days per month (MDM) after 8 weeks of supplementation. Participants will: Orally consume two caps of each product (taken at the same time) daily, one in the morning and one at the lunchtime preferably during meal, for 8 weeks after a running period of 8 weeks without supplementation. Intake will be initiated from the day of follow-up visit (V1) after all study procedures being performed until the day of the end-of-study visit (V2).

Állapot (regiszter)
Toboroz
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
120 (tervezett)
Első benyújtás
2025. máj. 19.
Kezdés
2025. máj. 15.
Elsődleges befejezés
2025. dec. 15.
Fő szponzor
Benfida, a department of Handi-Move
Betegségek
Migrén
NCT-szám
NCT07015411

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 120
  • 2025. máj. 15. és az elsődleges befejezés (2025. dec. 15.) között
  • 1 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.

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Korábbi kezelés

  • Medication overuse for headache defined as acute headache medication >10-15 days per month depending on the half-life of the medication (left to PI discretion);
  • Bariatric surgery;
  • Concurrent participation in another clinical study or having participated in the last 3 months:
  • Chronic drug and alcohol abuse;

Más betegség

  • Other primary head pain disorders such as but not restricted to tension-type headache, cluster headache, fibromyalgia;
  • Secondary head pain due to trauma, injury, infections;
  • Severe medical conditions affecting absorption and metabolism of the product, including but not restricted to chronic use of laxatives;
  • Severe psychiatric conditions that could interfere with diary compliance or assessment of the product (e.g., severe depression or cognitive impairments) left to investigator discretion;
  • Specific allergies or intolerance to components of the product;
  • Swallowing disorders;
  • Hepatic or biliar truct disorders;
  • Active malignancy and immunosuppression therapy;

Egyéb

  • Use of other dietary supplements that could potentially affect migraines, unless willing to discontinue them before the study begins (wash out period of 3 months);
  • Women who are pregnant, breastfeeding, or planning to become pregnant during the study period;
  • Women of childbearing potential without medically effective form of contraception unless they can confirm they've had bilateral tubal ligation or that their male partner has had a vasectomy;
  • Recent migraine interventions: Such as Botox injections (except if considered as a stable treatment, i.e. not the first injection), nerve blocks, or other invasive treatments in the last 6 months;
  • Anticoagulants (coumarin compound);
  • Hypothyroidism;
  • Close collaborators of investigational team, of sponsor or of study coordinator;
  • Under guardianship or judiciable protection.

Kiket keres a vizsgálat

  • Male or female between 18 and 75 years;
  • Diagnosis of migraine meeting the criteria of the International Classification of Headache Disorders (ICHD-3) (with or without aura)
    • At least 5 attacks fulfilling the criteria below
    • Headache attacks lasting 4-72 hours (untreated or unsuccessfully treated)
    • Headache has at least two of the following characteristics
    • unilateral location
    • pulsating quality
    • moderate or severe pain intensity
    • aggravation by or causing avoidance of routine physical activity (eg, walking or climbing stairs)
    • During headache at least one of the following:
    • nausea and/or vomiting
    • photophobia and phonophobia
    • Not attributed to another disorder
  • Migraine frequency of at least 6 headache days per month during the last 3 months;
  • Stable body mass index (BMI) between 18.5-35.0;
  • Stable medication use with no significant changes in prophylactic or acute migraine treatments in the past 3 months, and willingness to maintain or reduce (if not needed) this throughout the study period;
  • Willingness and ability to complete an ediary (mobile app or web based) and to follow the instruction of the study;
  • Having signed an informed consent.

Életkor a regiszterben: 18 év – 75 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

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