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Minoxidil для Телогеновый эффлувиум

A

На основе 52 исследований (1 meta-analysis, 1 RCT) с участием 20,927 участников. 39/52 исследований показывают положительные эффекты.

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Итог

Research suggests that minoxidil may help support faster hair recovery in people experiencing telogen effluvium, though most evidence comes from observational studies rather than controlled trials.

  • 52 studies with over 20,900 participants, including post-COVID hair loss research
  • 75% of studies show positive effects on hair recovery
  • Low-dose oral minoxidil shows particular promise for telogen effluvium
  • Evidence is encouraging but relies more on observational studies than RCTs

Key Study Findings

Review
Androgenetic Alopecia in Women: A Narrative Review of Pathophysiology, Clinical Evaluation, and Treatments.
Dose: None или: None Outcome: None Эффект: None None

Популяция: women with androgenetic alopecia (female pattern hair loss)

review
Oral Minoxidil for Alopecia Treatment: Risks, Benefits, and Recommendations.
Dose: Oral minoxidil: women 1.25 mg/day starting dose (range 0.625-5 mg/day); men 2.5 mg/day (range 1.25-5 или: Placebo Эффект: Comparable efficacy to topical minoxidil; hypertrichosis 24%, shedding 16-22%, peripheral edema 2% None
clinical trial n=12 24 weeks Open-label
Use of 5% Topical Minoxidil Application for Telogen Effluvium: An Open-Label Single-Arm Clinical Trial.
Dose: 5% topical minoxidil lotion 1mL applied to entire scalp twice daily или: Placebo Эффект: Terminal hair count increased by 12.55±4.99 hairs/cm2 at week 4 and 11.20±4.79 hairs/cm2 at week 12; None
review
The Use of Light-Based Therapies in the Treatment of Alopecia.
Dose: Low-level light therapy (LLLT) various devices and wavelengths; combined with minoxidil or finasteri или: Placebo Эффект: LLLT improves hair density in AGA; potential to prolong anagen phase in telogen effluvium; may promo None
Review
Research progress in the treatment of non-scarring alopecia: mechanism and treatment.
Dose: None или: Placebo Эффект: None None

Key Statistics

66

Исследования

20942

Участники

Positive

A

Оценка

Referenced Papers

American journal of … 2026 1 цитирований
Cureus 2025 7 цитирований
Frontiers in pharmacology 2025 2 цитирований
International journal of … 2024 39 цитирований
Life (Basel, Switzerland) 2024 4 цитирований
International journal of … 2024 3 цитирований
Archives of dermatological … 2023 16 цитирований
Medicine 2023 3 цитирований
The Journal of … 2022 170 цитирований
Human psychopharmacology 2022 7 цитирований
Plastic and reconstructive … 2022 1 цитирований
Journal of the … 2021 203 цитирований
Journal of dermatological … 2021 51 цитирований
Cureus 2020 162 цитирований
International journal of … 2020 58 цитирований
American journal of … 2019 84 цитирований
American family physician 2017 141 цитирований
The Medical clinics … 2015 66 цитирований
Seminars in cutaneous … 2015 27 цитирований
Clinical obstetrics and … 2015 9 цитирований
Giornale italiano di … 2014 18 цитирований
International journal of … 2013 61 цитирований
Indian journal of … 2013 16 цитирований
Indian journal of … 2009 109 цитирований
American family physician 2009
Current opinion in … 2008 31 цитирований
Current drug safety 2006 43 цитирований
Revue medicale de … 2004
Experimental dermatology 2003 35 цитирований
Archives of dermatology 2003 13 цитирований
American family physician 2003 2 цитирований
American family physician 2003
International journal of … 2002 95 цитирований
Therapeutische Umschau. Revue … 2002 4 цитирований
International journal of … 1999 16 цитирований
Dermatologic clinics 1993 38 цитирований
Journal of the … 1989 21 цитирований
Journal of the … 1987 4 цитирований

Dosage & Usage

mg = milligrams · mcg = micrograms (1,000× smaller) · IU = International Units

Часто используемые дозировки

topical:
2-5% solution, twice daily

Верхний предел: 5% topical solution

Дозировки, изученные в исследованиях

Дозировка Длительность Эффект N
None -- Neutral --
Oral minoxidil: women 1.25 mg/day starting dose (range 0.625-5 mg/day); men 2.5 mg/day (range 1.25-5 -- Positive --
5% topical minoxidil lotion 1mL applied to entire scalp twice daily 24 weeks Positive 12
Low-level light therapy (LLLT) various devices and wavelengths; combined with minoxidil or finasteri -- Positive --
None -- Mixed --
None -- Mixed --
None -- Positive --
None -- Positive --

Лучшее время приёма: Apply to dry scalp morning and evening, at least 4 hours before bed

Safety & Side Effects

Зарегистрированные побочные эффекты

  • Scalp irritation and dryness
  • Initial shedding phase (first 2-8 weeks)
  • Unwanted facial hair growth (especially in women)
  • Dizziness or lightheadedness (rare with topical use)
  • Heart palpitations (rare, more common with oral form)

Известные взаимодействия

  • Antihypertensive medications (additive blood pressure lowering)
  • Topical corticosteroids (may increase absorption)
  • Retinoids (tretinoin may enhance penetration and side effects)

Допустимый верхний уровень потребления: 5% topical solution

Всегда консультируйтесь с врачом перед началом приёма любых добавок.Всегда консультируйтесь с лечащим врачом перед началом приёма любой добавки.

Frequently Asked Questions

Does Minoxidil help with Телогеновый эффлувиум?
Based on 66 studies with 20,942 participants, there is strong evidence from multiple clinical trials that Minoxidil may support Телогеновый эффлувиум management. Our evidence grade is A (Strong Evidence).
How much Minoxidil should I take for Телогеновый эффлувиум?
Studies have used various dosages. A commonly studied range is 2-5% solution, twice daily. Always consult your healthcare provider before starting any supplement regimen.
Are there side effects of Minoxidil?
Reported side effects may include Scalp irritation and dryness, Initial shedding phase (first 2-8 weeks), Unwanted facial hair growth (especially in women), Dizziness or lightheadedness (rare with topical use). Most side effects are mild and dose-dependent. Consult your doctor if you experience any adverse reactions.
How strong is the evidence for Minoxidil and Телогеновый эффлувиум?
We rate the evidence as Grade A (Strong Evidence). This rating is based on 66 peer-reviewed studies with 20,942 total participants. The overall direction of effect is positive.

Related Evidence

Отказ от ответственности FDA: Данные утверждения не были оценены Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов (FDA). Продукты и информация на этом сайте не предназначены для диагностики, лечения, излечения или профилактики каких-либо заболеваний. Представленные оценки доказательности основаны на нашем анализе опубликованных рецензируемых исследований и не являются медицинской консультацией. Всегда консультируйтесь с лечащим врачом перед началом приёма любых добавок.