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34 studies found for:    Open Studies | "Alopecia"
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Open Studies | "Alopecia" (34 records)
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Rank Status Study
1 Recruiting A Pilot Study of Tralokinumab in Subjects With Moderate to Severe Alopecia Areata
Condition: Alopecia Areata
Interventions: Drug: Tralokinumab;   Drug: Placebo
2 Recruiting Topical Garlic Concentrate for Alopecia Areata in Children
Condition: Alopecia Areata
Intervention: Drug: garlic concentrate
3 Recruiting Excimer Light for Alopecia Areata
Condition: Alopecia Areata
Intervention: Procedure: UVB excimer light
4 Recruiting Efficacy, Safety and Tolerability of CG428 Cutaneous Solution on Chemotherapy Induced Alopecia; Controlled Study (ELAN)
Condition: Alopecia
Interventions: Drug: CG 428 cutaneous solution;   Drug: Placebo cutaneous solution
5 Recruiting Intralesional Steroids in the Treatment of Alopecia Areata
Condition: Alopecia Areata
Interventions: Drug: Intralesional Triamcinolone 2.5 mg/ml;   Drug: Intralesional Triamcinolone 5 mg/ml;   Drug: Intralesional Triamcinolone 10 mg/ml;   Drug: Intralesional Saline
6 Not yet recruiting Evaluate the Clinical Effectiveness of RegenKit Platelet-rich Plasma (PRP) in Androgenetic Alopecia Treatment
Condition: Androgenetic Alopecia
Interventions: Device: Autologous Platelet Rich Plasma;   Device: Saline solution injection
7 Recruiting Phase 2A Study of Setipiprant Tablets in Androgenetic Alopecia in Males
Condition: Alopecia
Interventions: Drug: setipiprant;   Drug: placebo;   Drug: finasteride
8 Recruiting "Impact of Chemotherapy-induced Alopecia on the Quality of Life of Women With Breast Cancer"
Condition: Chemotherapy-induced Alopecia
Intervention: Behavioral: Semi-structured interviews
9 Recruiting Biocellular-Cellular Regenerative Treatment Scaring Alopecia and Alopecia Areata
Conditions: Alopecia Areata;   Scarring Alopecia
Interventions: Procedure: tSVF by lipoaspiration;   Procedure: PRP Concentration;   Procedure: Emulsification tSVF;   Procedure: cSVF isolation and concentration;   Procedure: cSVF in Normal Saline IV
10 Recruiting Study To Evaluate The Efficacy And Safety Profile Of PF-06651600 And PF-06700841 In Subjects With Alopecia Areata
Condition: Alopecia Areata
Interventions: Drug: PF-06651600;   Drug: PF-06700841;   Drug: Placebo
11 Not yet recruiting Safety and Efficacy Study of SHAPE Gel in Alopecia Areata
Condition: Alopecia Areata
Intervention: Drug: SHAPE Gel
12 Not yet recruiting Study to Assess the Efficacy of Intralesional Corticosteroid on the Treatment of Frontal Fibrosing Alopecia
Condition: Frontal Fibrosing Alopecia
Intervention: Other: Corticosteroid/Saline
13 Recruiting TREg Activation in the Treatment of the PELADE (Alopecia Areata)
Condition: Alopecia Areata
Interventions: Drug: IL2;   Drug: placebo
14 Recruiting The Effect of Platelet-rich Plasma in Subjects With Androgenetic Alopecia
Condition: Androgenetic Alopecia
Interventions: Device: Platelet Rich Plasma Prep System;   Drug: Placebo
15 Recruiting Study to Evaluate the Efficacy and Safety of P-3074 Topical Solution in the Treatment of Androgenetic Alopecia
Condition: Alopecia, Androgenetic
Interventions: Drug: P-3074;   Drug: Finasteride;   Drug: Vehicle
16 Recruiting Efficacy Study of a Cosmetic Lotion in the Treatment of Alopecia Areata in Males and Females
Condition: Alopecia Areata
Intervention: Other: MEXIS/M6S Patent - lotion against alopecia
17 Recruiting PAI-1 Expression in Non-scarring Hair Loss
Conditions: Androgenetic Alopecia;   Telogen Effluvium;   Alopecia Areata
Intervention:
18 Not yet recruiting Hairstetics™ Anchoring System in Female Pattern Hair Loss (HAS-FPHL)
Conditions: Female Pattern Baldness;   Alopecia, Androgenetic
Intervention: Device: Hairstetics™ anchoring system
19 Recruiting Study to Evaluate a Nutraceutical Supplement for Treatment of Hair Loss and Thinning in Females
Condition: Hair Loss
Interventions: Dietary Supplement: Nutrafol;   Dietary Supplement: placebo
20 Not yet recruiting Pharmacokinetics/ Pharmacodynamics and Safety of DA-4001 in Healthy Male Subjects With Androgenic Alopecia
Condition: Androgenic Alopecia
Interventions: Drug: DA-4001 H;   Drug: DA-4001 L

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Study has passed its completion date and status has not been verified in more than two years.