Clinical Trials Directory

Trials / Completed

CompletedNCT01931748

A Randomized, Double-Blind, Parallel, Non-Inferiority, Multicenter Trial Evaluate the Efficacy and Safety of UNCNT Compared to MELSMON in Female With Menopausal Syndrome

Study of Non-inferiority UNCNT Versus MELSMON in Female With Menopausal Syndrome: Randomized Confirmatory Clinical Trial

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
104 (actual)
Sponsor
Unimed Pharmaceuticals · Industry
Sex
Female
Age
40 Years
Healthy volunteers
Not accepted

Summary

The Purpose of this study is to evaluate in a randomized, double-blind, Parallel, Non-inferiority, Multicenter, the efficacy and safety of UNCNT in comparison to the active comparator of MELSMON in female having menopausal syndrome. Patients will be allocated randomly to receive either UNCNT or MELSMON. Through the injection of UNCNT to female having menopausal disorder, efficacy in the improvement of the menopausal symptoms by Kupperman index is to be evaluated and compared with MELSMON.

Conditions

Interventions

TypeNameDescription
DRUGMELSMON
DRUGUNCNT

Timeline

Start date
2013-04-01
Primary completion
2014-04-01
Completion
2014-04-01
First posted
2013-08-29
Last updated
2014-05-08

Locations

2 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01931748. Inclusion in this directory is not an endorsement.

A Randomized, Double-Blind, Parallel, Non-Inferiority, Multicenter Trial Evaluate the Efficacy and Safety of UNCNT Compa (NCT01931748) · Clinical Trials Directory