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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05846698
Other study ID # 2021-375
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2017
Est. completion date December 31, 2021

Study information

Verified date August 2023
Source First Affiliated Hospital of Chongqing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To investigate the effect of LBFKBRP on climacteric syndrome in women and explore its therapeutic mechanism.


Recruitment information / eligibility

Status Completed
Enrollment 276
Est. completion date December 31, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender Female
Age group 41 Years to 60 Years
Eligibility Clinical diagnosis of climacteric syndrome

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Luo-Bu-Fu-Ke-Bi-RI Pill
10 pills twice daily
tibolone
2.5 mg once daily

Locations

Country Name City State
China The First Affiliated Hospital of Chongqing Medical University Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Guoqing Zhou

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sex hormone 3 month
See also
  Status Clinical Trial Phase
Completed NCT06057896 - Effects of Combined Natural Molecules on Metabolic Syndrome in Menopausal Women
Not yet recruiting NCT06419972 - Multimodal Program for Climacteric Women N/A
Completed NCT01275807 - Effectiveness and Safety of Acupuncture for Climacteric Syndrome in Patients With Breast Cancer Phase 4
Recruiting NCT06136208 - Pharmacokinetic Aspects of 25-mg Estradiol Pellet in Climacteric Women N/A
Withdrawn NCT01695616 - Efficacy and Safety of Passiflora Incarnata and Isoflavona Combination in the Treatment of Climacteric Symptoms Phase 3
Completed NCT03118908 - Clinical Evaluation of Effectiveness and Safety of Amberen and Smart B by Women With Climacteric Syndrome N/A