Skip to main content
MedPathMedPath Home
Clinical Trials/IRCT20190210042676N18
IRCT20190210042676N18
Recruiting
Phase 2

Clinical evaluation of the safety and effectiveness Oral capsules (containing minoxidil, finasteride and biotin) in the prevention and treatment of androgenic hair loss

Knowledge-based company of Janus0 sites20 target enrollmentTBD
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Knowledge-based company of Janus
Enrollment
20
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
Knowledge-based company of Janus

Eligibility Criteria

Inclusion Criteria

  • •Male aged 18\-50 years
  • •General health
  • •Hair Loss Status II, III, IV Based on Norwood Scale
  • •Voluntary participation and signing written informed consent

Exclusion Criteria

  • •Chronic active scalp disease other than hair loss
  • •Using any prescribed drug or OTC for hair loss within the past 3 months
  • •Documented sensitivity to formulation components
  • •Any severe weight loss or strict diet therapy during the study

Outcomes

Primary Outcomes

Not specified

Similar Trials

Active, not recruiting
Not Applicable
Clinical Evaluation of the AqueSys Implant for the Treatment of ocular hypertension and open angle glaucomaOcular hypertension and open angle glaucomaEye - Diseases / disorders of the eye
ACTRN12610000021077Aquesys Inc20
Recruiting
Phase 2
Clinical evaluation of the safety and effectiveness of the nanofiber undereye pad to improve surface wrinkles and dark circles under the eyes
IRCT20210130050179N9ano tarpak company10
Completed
Not Applicable
Clinical Evaluation of the Safety and Effectiveness of Harvest Autologous Platelet Concentrate and Harvest Autologous Thrombin for Treatment of Lower Extremity Chronic Diabetic Ulcers
ISRCTN28965380Harvest Technologies Corp. (USA)59
Not yet recruiting
Phase 4
a clinical trial to compare efficacy of the analgesic activity of inj. Bupivacaine vs inj. Ropivacaine given at transverse abdominis block and also compare the safety parameters also.
CTRI/2017/08/009249Department of Anaesthesiology
Not yet recruiting
Not Applicable
Clinical evaluation of the safety and the usefulness of robot assisted lung lobectomy with nodal dissection for primary lung cancer.Primary lung cancer
JPRN-UMIN000012103Department of Surgery and Clinical Science, Yamaguchi University Graduate School of Medicine.10