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

NCT05312190 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 330

Last updated 2022-04-05

No results posted yet for this study

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.

Conditions

  • Menstrual Disorders

Interventions

DRUG

ZhenQi 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.

DRUG

Progesterone 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 & Collaborators

  • West China Second University Hospital

    collaborator OTHER
  • Chongqing Medical University No.1 Affiliated Hospital

    collaborator UNKNOWN
  • The Second Hospital of Hebei Medical University

    collaborator OTHER
  • Second Affiliated Hospital of Nanchang University

    collaborator OTHER
  • Zhongda Hospital

    collaborator OTHER
  • Hubei Maternal and Child Health Hospital

    collaborator UNKNOWN
  • Liuzhou Maternity and Child Healthcare Hospital

    collaborator OTHER
  • Zhejiang University Medical College Affiliated Hangzhou First People's Hospital

    collaborator UNKNOWN
  • Guangzhou Women and Children's Medical Center

    collaborator OTHER
  • Peking Union Medical College Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-15
Primary Completion
2022-12-30
Completion
2023-06-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05312190 on ClinicalTrials.gov