Actively Recruiting
Real-world Evaluation of Qingxin Zishen Decoction on Ovarian Reserve Function Clinical Efficacy in Patients With Decreased
Led by Yun Chen · Updated on 2024-04-04
178
Participants Needed
1
Research Sites
165 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A prospective cohort study evaluated the clinical efficacy of Qingxin Zishen Decoction
CONDITIONS
Official Title
Real-world Evaluation of Qingxin Zishen Decoction on Ovarian Reserve Function Clinical Efficacy in Patients With Decreased
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female aged between 25 and 45 years old
- AMH level less than 1.1 ng/ml
- Antral follicle count (AFC) less than 5 to 7 on both ovaries
- Basal FSH level of 10 IU/L or higher for two consecutive menstrual cycles
You will not qualify if you...
- Reduced ovarian function caused by ovarian or uterine surgery, radiotherapy, or chemotherapy
- Liver function (AST or ALT) or renal function (BUN or Ccr) greater than twice the normal value
- History of mental illness or legal disability
- Use of endocrine-affecting drugs, estrogen, progesterone, oral contraceptives, or related Chinese medicines within 3 months before the study
- Unexplained irregular vaginal bleeding
- Participation in other clinical drug trials
- Women who want to have children but whose spouse's semen test does not meet the standard
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Jiangsu Provincial Hospital of Traditional Chinese Medicine Affiliated to Nanjing University of Chinese Medicine
Nanjing, Jiangsu, China, 210023
Actively Recruiting
Research Team
C
Chen Yun
CONTACT
T
TEO YONG QING
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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