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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01852487
Other study ID # Pumpkin0912
Secondary ID
Status Completed
Phase N/A
First received May 9, 2013
Last updated May 10, 2013
Start date February 2012
Est. completion date December 2012

Study information

Verified date May 2013
Source Dream Plus
Contact n/a
Is FDA regulated No
Health authority Korea: Ministry of Education, Science, and Technology
Study type Interventional

Clinical Trial Summary

Androgenic alopecia is the most common cause of hair loss in men. Finasteride and minoxidil are available in treatment of androgenetic alopecia, although the former causes decreased libido or ejaculate volume, erectile dysfunction, the latter causes scaling, itching of the scalp. Recently, Pulpkin Seed Oil shows some improved clinical efficacy on scalp hair growth in men with androgenetic alopecia, but there is no evidence to support this.

The investigators conducted a randomized, double-blind, placebo-controlled efficacy and tolerability trial of Pumpkin seed oil (400mg/day)therapy in male patients with androgenetic alopecia.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- 18 to 65 years of age

- Androgenetic alopecia of Norwood-Hamilton scale grade II-V

Exclusion Criteria:

- Severe medical problems including renal problems, prostate diseases, diabetes mellitus o

- Patients who took any medicine which can affect the hair growth in recent 3 months.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
400mg /day during 6 months


Locations

Country Name City State
Korea, Republic of Pusan National University Yangsan Hospital Yangsan Gyeongsangnam-do

Sponsors (1)

Lead Sponsor Collaborator
Dream Plus

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Other hair analysis using phototrichogram at weeks 12 and 24 No
Primary investigator assessment score using photographs of scalp hair at weeks 12 and 24 No
Secondary patient self-assessment scores at weeks 12 and 24 No
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