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Clinical Trials/ITMCTR2000003596
ITMCTR2000003596
Not yet recruiting
Phase 1

Traditional Chinese medicine formulation combined with promestriene in the treatment of genitourinary syndrome of menopause (GSM) : a randomized, double-blind, controlled clinical trial

International Peace Maternity & Child Health Hospital affiliated with Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
genitourinary syndrome of menopause, GSM
Sponsor
International Peace Maternity & Child Health Hospital affiliated with Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Female

Investigators

Sponsor
International Peace Maternity & Child Health Hospital affiliated with Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China

Eligibility Criteria

Inclusion Criteria

  • 1\.2 inclusion criteria
  • 1\.2\.1 the postmenopausal women meeting the GSM diagnostic criteria and age over 40 years old
  • 1\.2\.2 the people of no use of hormonal drugs at least 3 months
  • 1\.2\.3 the people volunteered for the experiment, and signed the informed consent

Exclusion Criteria

  • 1\.3 exclusion standard
  • 1\.3\.1the people without sexual partners because of unmarried, divorced, widowed and other reasons
  • 1\.3\.2 the people who use GnRH \- a or steroid hormone in three months
  • 1\.3\.3 the people who place levonorgestrel intrauterine sustained release system into uterus
  • 1\.3\.4 the people who have severe disease about heart and cerebral vessels or liver or kidney or diabetes or malignant tumor or the others.
  • 1\.3\.5 the people who affect cognition on account of mental disorder or medicine or chronic drinking
  • 1\.3\.6 the people who have coagulation dysfunction or thrombotic disease
  • 1\.3\.7 the people who participate in other drug clinical trials

Outcomes

Primary Outcomes

Not specified

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