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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01822288
Other study ID # 101080-F
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date November 16, 2012
Est. completion date August 26, 2021

Study information

Verified date December 2021
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Menopausal syndromes includes somatic symptom, psychosomatic symptoms, sexual dysfunction and even urinary symptoms. Hormone therapy (HT) is widely used for controlling menopausal symptoms. Common HT for menopausal syndrome with intact uterus includes tibolone, estradiol valerate (E2V) 1mg & medroxyprogesterone acetate (MPA) 2.5 mg, and conjugated equine estrogens & MPA. However, only a few literatures mentioned about the therapeutic effect of tibolone, but lack of comparison research about their therapeutic effect on somatic symptoms, psychosomatic symptoms, sexual dysfunction and even urinary symptoms. The knowledge of the above therapeutic effects should be important for choosing a suitable medication. Therefore, the aim of this study is to assess the therapeutic effect on somatic symptoms, psychosomatic symptoms, sexual dysfunction and even urinary symptoms between tibolone and E2V/MPA.


Recruitment information / eligibility

Status Completed
Enrollment 125
Est. completion date August 26, 2021
Est. primary completion date July 8, 2021
Accepts healthy volunteers No
Gender Female
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - All female patients with intact uterus who seek for medical treatment for menopausal syndrome Exclusion Criteria: - patients with gynecologic or breast cancers

Study Design


Intervention

Drug:
Tibolone
Tibolone 2.5 mg once a day for patients with menopausal syndrome (self-paid)
Estradiol & medroxyprogesterone acetate
Estradiol & medroxyprogesterone acetate once a day for patients with menopausal syndromes, for patients without the need for self-paid drug

Locations

Country Name City State
Taiwan Far Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)

Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Menopausal symptoms To clarify any difference of reduction in menopausal symptom scores between these two groups 12 weeks
Secondary sexual function To clarify any difference of improvements of sexual function scores between these two groups 12 weeks
Secondary lower urinary tract symptoms To clarify any difference of improvements of lower urinary tract symptoms scores between these two groups 12 weeks
Secondary psychosomatic symptoms To clarify any difference of improvements of psychosomatic symptoms scores between these two groups 12 weeks