Efficacy and Safety for Cimicifuga/Hypericum Product — CH  

Perimenopausal Disorder Clinical Trial

Official title: Phase 3 Study - Efficacy and Tolerance for the Mixture of Dry Extracts Black Cohosh and Saint John's Worth Versus Isolated Black Cohosh Extract for the Climacteric Symptoms' Control

Status Not yet recruiting

Clinical Trial Summary

Climacteric Complains bring to women many problems for living a normal life - hot flashes, irritation are 2 of many problems and the mixture of those 2 plant extract must bring a new horizon for this part of time.

Clinical Trial Description

2 herbal extracts used in general alone will be running together for the best climacteric women on quality of life.

The investigators will test the mixture already in the market as GynoPlus and RemifeminPlus, but as each extract has its own particularities the investigators will try CIM/HIP as a unique formulation versus Clifemin® as control and Aplause® as comparator.

This protocol was performed for the best of our volunteers. ;

Study Design

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

Related Conditions & MeSH terms

• Perimenopausal Disorder

• NCT number: NCT01481025
• Study type: Interventional
• Source: Phytopharm Consulting Brazil
• Contact: Marli Chaves, Secretary
• Phone: +55 51 8130-8454
• Email: contato@phytopharm.com.br
• Status: Not yet recruiting
• Phase: Phase 3
• Start date: November 2011
• Completion date: August 2012