Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Endometriosis
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 40 years
Gender
Only males

Description

Women with endometrioma will be randomised into either the experimental group or the placebo comparator group in a 1:1 ratio. The subjects will be given SUNPHENON EGCg or placebo for 3 months prior to their planned surgery.

Women with endometrioma will be randomised into either the experimental group or the placebo comparator group in a 1:1 ratio. The subjects will be given SUNPHENON EGCg or placebo for 3 months prior to their planned surgery.

Tracking Information

NCT #
NCT02832271
Collaborators
  • Chinese Academy of Medical Sciences
  • Sun Yat-sen University
  • Guangdong Provincial Hospital of Traditional Chinese Medicine
  • Jiangxi University of Traditional Chinese Medicine
Investigators
Principal Investigator: Ronald Wang, MD PhD Chinese University of Hong Kong