Skip to content

Clinical and Basic Researches Related to ZhenQi Buxue Oral Liquid in Treating Menstrual Disorders

Clinical and Basic Researches Related to ZhenQi Buxue Oral Liquid in Treating Menstrual Disorders

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05312190
Enrollment
330
Registered
2022-04-05
Start date
2022-03-15
Completion date
2023-06-30
Last updated
2022-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Menstrual Disorders

Keywords

Menstrual disorders, Traditional Chinese medicine

Brief summary

This study is a national multicenter prospective, randomized, controlled trial, which evaluates Zhenqi Buxue Oral Liquid,Progesterone Capsules and the addition of Zhenqi Buxue Oral Liquid to Progesterone Capsules in the treatment of menstrual disorders in adults women. One third of participanta will receive Zhenqi Buxue Oral Liquid, one third of participanta will receive Progesterone Capsules, and the another third will receive Zhenqi Buxue Oral Liquid and Progesterone Capsules in combination.

Detailed description

Menstrual disorders are one of the most common clinical symptoms in women. Since puberty, about 70% of women have experienced menstrual disorders, including early, delayed, shortened, prolonged, and more importantly oligomenorrhea, amenorrhea, and decreased menstrual flow.At present, the main method of western medicine for the treatment of menstrual disorders is hormone replacement therapy, but the incidence of adverse reactions is high, and the clinical effect is mediocre. Traditional Chinese medicine in my country mostly adopts holistic conditioning therapy for the treatment of irregular menstruation. Zhenqi Buxue Oral Liquid consists of sheep placenta, pearl, red ginseng, wolfberry, astragalus, angelica, coix seed, ginger and jujube. The excipients are protein sugar and sodium benzoate. Nourishes qi and blood. It is suitable for dizziness, pale complexion, fatigue, lack of energy and lazy words caused by insufficient qi and blood. This study will conduct a comprehensive and in-depth study on its treatment of mental and psychological stress and menstrual disorders with oligomenorrhea, amenorrhea, amenorrhea and decreased menstrual flow as the main manifestations. The molecular mechanism and clinical improvement, and the safety and adverse reactions of its use paln to be clarified.

Interventions

DRUGZhenQi BuXue KouFuYe

Zhenqi Buxue Oral Liquid consists of sheep placenta, pearl, red ginseng, wolfberry, astragalus, angelica, coix seed, ginger and jujube. The excipients are protein sugar and sodium benzoate. Nourishes qi and blood. It is suitable for dizziness, pale complexion, fatigue, lack of energy and lazy words caused by insufficient qi and blood.

DRUGProgesterone Capsules

The main ingredient of Progesterone Capsules is abbsolutely progesterone,a kind of hormone,which is the main method of western medicine for the treatment of menstrual disorders

Sponsors

West China Second University Hospital
CollaboratorOTHER
Chongqing Medical University No.1 Affiliated Hospital
CollaboratorUNKNOWN
The Second Hospital of Hebei Medical University
CollaboratorOTHER
Second Affiliated Hospital of Nanchang University
CollaboratorOTHER
Zhongda Hospital
CollaboratorOTHER
Hubei Maternal and Child Health Hospital
CollaboratorUNKNOWN
Liuzhou Maternity and Child Healthcare Hospital
CollaboratorOTHER
Zhejiang University Medical College Affiliated Hangzhou First People's Hospital
CollaboratorUNKNOWN
Guangzhou Women and Children's Medical Center
CollaboratorOTHER
Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Intervention model description

This study is a national multicenter prospective, randomized, controlled trial. One third of participanta will receive Zhenqi Buxue Oral Liquid, one third of participanta will receive Progesterone Capsules, and the another third will receive Zhenqi Buxue Oral Liquid and Progesterone Capsules in combination.

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

1. Aged between 25 and 40 years old; 2. Patients with oligomenorrhea or oligomenorrhea or menopause within three months (see Appendix 1: Diagnostic Criteria of Traditional Chinese and Western Medicine) 3. Meet the clinical medication conditions for progesterone to regulate menstruation 4. The research subjects were informed and voluntarily participated in this study, and signed the informed consent at the same time.

Exclusion criteria

1. Age \<25 years or \>40 years old, pregnant or breastfeeding women 2. Ovarian dysfunction caused by local ovarian surgery, radiotherapy and chemotherapy for previous malignant tumors, taking hormones or immunosuppressive drugs; 3. Combined with serious or unstable physical diseases that may affect the efficacy of drugs and the conduct of trials, including liver, kidney, gastrointestinal, cardiovascular, respiratory, endocrine, neurological, immune or blood system diseases, etc., mental patients . 4. Those who were allergic to the drugs used in the trial or had serious adverse reactions in the past; 5. Breast cancer or family history of breast cancer in first-degree relatives, irregular vaginal bleeding, uterine fibroids (≥3cm), endometriosis, atypical endometrial hyperplasia, endometrial cancer and other hormone-dependent reproduction Systemic diseases and other malignant tumors; 6. Those with a history of thromboembolic disease or thrombosis; 7. Participated in a clinical trial of another research drug within 3 months prior to inclusion in this study (the first interview); 8. Those who have used related drugs in the past 3 months or have abused or depended on substances (alcohol or drugs) in the past 3 months; heavy smokers (smokers who smoke 20 or more cigarettes per day); 9. Those who met the inclusion criteria, did not follow the doctor's advice, were unable to judge the curative effect or were unable to evaluate the curative effect due to incomplete data.

Design outcomes

Primary

MeasureTime frameDescription
Menstrual improvementWithin 3 months after the trial completeMenstrual improvement in cycle period

Secondary

MeasureTime frameDescription
Sex hormone levelsWithin 3 months after the trial completemainly FSH, LH,E2 and AMH
AFCWithin 3 months after the trial completeChanges in AFC in pelvic ultrasonography
SF-36Within 3 months after the trial completeThe change of the MOS item short from health survey

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026