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A camparative study effectiveness topical minoxidil nanosuspention and minoxidil %2 solution in the treatment of alopecia androgenetic

A camparative study effectiveness topical minoxidil nanosuspention and minoxidil 2% solution in the treatment of alopecia androgenetic

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180120038450N1
Enrollment
140
Registered
2018-07-10
Start date
2018-06-13
Completion date
Unknown
Last updated
2018-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

alopecia areata.

Interventions

Intervention group: Topical minoxidil nanosuspention.

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Signature of written consent for participation in the study 2-Age between 18-55 years 3-The presence of alopecia androgenetic in male or female 4-There is no other disorder that causes hair loss such as telogeny, echolinate or scarring hair (like lichen planus) Class 1-4 in the Fitzpatrick Classification for Skin Type and Grade 3-6 Hair Loss for Men in the Norwood Hamilton Classification and Grade 2-3 Hair Loss for Women in the Ludwing Classification, Non-Use of Finasteride, Anti-Androgenetics, Local Estrogen , Progesterone, tamoxifen, anabolic steroids, potent potent medications for hyperkeratosis, oral glucocorticoid, lithium, phenothiazines within 3 months before the start of the study

Exclusion criteria

Exclusion criteria: 1-Pregnancy 2-lactation 3-Using of anabolic steroids in the last 6month 4-Using of topical minoxidil in the last 6month 5-Using of antiandrogenetic drugs in the last 6 month 6-Using of the drugs who make hyper keratosis as like as systemic corticosteroids in the last 6 month 7-Dont be principled to curative protocol 8-Hair transplantation 9-Collagen vascular disease or HIV 10-Endocrinopathy like PCO, Hypotyroid

Design outcomes

Primary

MeasureTime frame
Hair density. Timepoint: 0,2,4,6 months. Method of measurement: Phototyrographic method.;Diagonal hair shaft. Timepoint: 0,2,4,6. Method of measurement: Phototyrographic method.;Patient satisfaction. Timepoint: 2,4,6 months. Method of measurement: questionnaire.

Secondary

MeasureTime frame
Headache. Timepoint: 2,4,6 months. Method of measurement: Ask the patient.;Erythema - redness-itching. Timepoint: 0,2,4,6 month. Method of measurement: Ask the patient.;Hypopigmentation, hyperpigmentation. Timepoint: 0,2,4,6 month. Method of measurement: Evaluate by observation and Ask the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahla Mirzaeei

Kermanshah University of Medical Sciences

shahlamirzaeei@gmail.com+98 83 3427 6480

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026