Skip to main content
HairCited

スピロノラクトン 女性型脱毛症

A

合計5,743名の参加者を対象とした19件の研究(メタアナリシス2件、RCT 4件を含む)に基づく。19件中16件の研究で肯定的な効果が示されている。

<\/script>\n
`; }, get iframeSnippet() { const domain = 'haircited.com'; const params = 'ingredient\u003Dspironolactone\u0026condition\u003Dfemale\u002Dpattern\u002Dhair\u002Dloss'; return ``; }, get activeSnippet() { return this.method === 'script' ? this.scriptSnippet : this.iframeSnippet; }, copySnippet() { navigator.clipboard.writeText(this.activeSnippet).then(() => { this.copied = true; setTimeout(() => { this.copied = false; }, 2000); }); } }" @keydown.escape.window="open = false" @click.outside="open = false">

Embed This Widget

Style



      
      
    

Widget powered by . Free, no account required.

A

結論

Spironolactone is strongly supported by research as an effective option that may help women with female pattern hair loss, with both oral and topical formulations showing benefits in clinical trials.

  • 84% of studies show positive effects, including 4 RCTs focused on women
  • Both oral and topical formulations have demonstrated benefits
  • A dedicated meta-analysis confirms efficacy and safety in female pattern hair loss
  • Combination with minoxidil may offer enhanced results

Key Study Findings

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

対象集団: women with androgenetic alopecia (female pattern hair loss)

Randomized Controlled Trial n=204 24 weeks Double-blind
Spironolactone versus Bicalutamide in female pattern hair loss: A randomised clinical trial.
Dose: Bicalutamide 50 mg/day; spironolactone 100 mg/day vs: Spironolactone 100 mg/day Outcome: Hair density and shaft diameter change at 24 … 効果: Frontal: +5.05 vs +3.13 hairs/cm2 (diff 1.92) P < 0.001 (frontal); P = 0.028

対象集団: Women 18-50 with Sinclair Grade II-V FPHL (India)

randomized controlled trial n=80 24 weeks Single-blind
Evaluation of the Efficacy and Safety of Topical Spironolactone versus Topical Minoxidil in the Treatment …
Dose: Group A: 1% topical spironolactone gel twice daily; Group B: 5% topical minoxidil gel twice daily vs: Placebo 効果: Both groups showed statistically significant improvement. Group A: 10 mild, 16 moderate, 2 excellent None
RCT n=48 24 weeks Double-blind
Efficacy and safety of oral spironolactone for female pattern hair loss in premenopausal women: a …
Dose: Spironolactone 100 mg once daily vs: Placebo 効果: Terminal hair counts: 9.48 vs 5.32 hairs/cm2; hair diameter: 4.23 vs 2.96 μm; moderate-to-marked imp p=0.063 (terminal hair counts)
Randomized Controlled Trial n=240 520 weeks Open-label
Nutritional deficiencies after sleeve gastrectomy and Roux-en-Y gastric bypass at 10 years: secondary analysis of …
Dose: None vs: Laparoscopic Roux-en-Y gastric bypass (LRYGB) Outcome: Nutritional deficiency prevalence at 10 years 効果: Iron deficiency: LSG 14% vs LRYGB 41% p=0.017 (iron deficiency)

対象集団: Severely obese adults undergoing bariatric surgery

Review
Male and female pattern hair loss.
Dose: None vs: Placebo 効果: None None

Key Statistics

45

研究数

6441

参加者数

Positive

A

グレード

Referenced Papers

Australian prescriber 2025 2 件の引用
Journal of cosmetic … 2023 3 件の引用
Journal of the … 2020 43 件の引用
Clinical and experimental … 2020 20 件の引用
Journal of the … 2019 55 件の引用
International journal of … 2018 129 件の引用
Australian journal of … 2018 8 件の引用
The Cochrane database … 2016 18 件の引用
The Medical clinics … 2015 66 件の引用
Journal of the … 2015 50 件の引用
Clinical obstetrics and … 2015 9 件の引用
Current problems in … 2015 8 件の引用
Der Hautarzt; Zeitschrift … 2013 19 件の引用
International journal of … 2013
The Australasian journal … 2011 44 件の引用
Skinmed 2010 33 件の引用
The Australasian journal … 2009 31 件の引用
Seminars in cutaneous … 2009 4 件の引用
The Australasian journal … 2007 32 件の引用
Duodecim; laaketieteellinen aikakauskirja 2006
Journal of the … 2005 247 件の引用
The British journal … 2005 205 件の引用
Journal of the … 2005 64 件の引用

Dosage & Usage

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

一般的な使用量

hairloss:
100-200 mg/day (prescription)

上限量: 200 mg/day (hair loss indication)

研究で検討された用量

用量 期間 効果 N
None -- Neutral --
Bicalutamide 50 mg/day; spironolactone 100 mg/day 24 weeks Positive 204
Group A: 1% topical spironolactone gel twice daily; Group B: 5% topical minoxidil gel twice daily 24 weeks Positive 80
Spironolactone 100 mg once daily 24 weeks Positive 48
None 520 weeks Positive 240
None -- Positive --
Group A: topical finasteride 1% solution; Group B: topical spironolactone 5% solution; Group C: topi 16 weeks Positive 45
4 g -- Neutral --

推奨摂取タイミング: Once or twice daily with food; prescription required

Safety & Side Effects

報告されている副作用

  • Menstrual irregularities
  • Breast tenderness
  • Hyperkalemia (elevated potassium levels)
  • Dizziness and orthostatic hypotension
  • Frequent urination

既知の相互作用

  • ACE inhibitors and ARBs (increased hyperkalemia risk)
  • Potassium supplements and potassium-sparing diuretics (dangerous hyperkalemia)
  • NSAIDs (may reduce diuretic effectiveness and increase kidney risk)
  • Digoxin (spironolactone may increase digoxin levels)

耐容上限摂取量: 200 mg/day (hair loss indication)

サプリメントの摂取を開始する前に、必ず医療専門家にご相談ください。

Frequently Asked Questions

Does スピロノラクトン help with 女性型脱毛症?
Based on 45 studies with 6,441 participants, there is strong evidence from multiple clinical trials that スピロノラクトン may support 女性型脱毛症 management. Our evidence grade is A (Strong Evidence).
How much スピロノラクトン should I take for 女性型脱毛症?
Studies have used various dosages. A commonly studied range is 100-200 mg/day (prescription). Always consult your healthcare provider before starting any supplement regimen.
Are there side effects of スピロノラクトン?
Reported side effects may include Menstrual irregularities, Breast tenderness, Hyperkalemia (elevated potassium levels), Dizziness and orthostatic hypotension. Most side effects are mild and dose-dependent. Consult your doctor if you experience any adverse reactions.
How strong is the evidence for スピロノラクトン and 女性型脱毛症?
We rate the evidence as Grade A (Strong Evidence). This rating is based on 45 peer-reviewed studies with 6,441 total participants. The overall direction of effect is positive.

Related Evidence

FDAに関する免責事項: これらの記述は米国食品医薬品局(FDA)による評価を受けていません。本ウェブサイトの製品および情報は、疾病の診断、治療、治癒、または予防を目的としたものではありません。表示されているエビデンスグレードは、公開された査読済み研究の分析に基づいており、医療上の助言を構成するものではありません。サプリメントの摂取を開始する前に、必ず医療専門家にご相談ください。