Skip to main content
Clinical Trials/ITMCTR2022000024
ITMCTR2022000024
Not yet recruiting
Phase 1

Clinical effect observation of kidney deficiency and blood stasis type of integrated Traditional Chinese and Western medicine by stages

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
intrauterine adhesions
Sponsor
Xiyuan Hospital,China Academy of Chinese Medical Sciences
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • (1\) Meet the diagnostic criteria of western medicine for intrauterine adhesions; (2\) Meet the diagnostic criteria of traditional Chinese medicine for intrauterine adhesions with kidney deficiency and blood stasis syndrome; (3\) Those who were diagnosed as moderate to severe adhesions during hysteroscopy (in the Chinese diagnostic grading standards for intrauterine adhesions) 9\-18 points for severe adhesion and 19\-28 points for severe adhesion); (4\) Those with fertility requirements; (5\) Age \=40 years old.

Exclusion Criteria

  • (1\) Congenital dysplasia of the uterus; combined with space\-occupying lesions in the uterine cavity, such as submucosal fibroids or endometrial polyps; (2\) ovulatory infertility; (3\) oligomenorrhea caused by low ovarian function; (4\) undiagnosed Vaginal bleeding (5\) known or suspected breast cancer; known or suspected precancerous lesions or malignant tumors affected by sex hormones; (6\) current or past history of liver tumors (benign or malignant); (7\) acute arterial thromboembolism, active venous thrombosis Formation, thromboembolic disease or medical history, high risk factors for venous or arterial thrombosis; ? severe hypertriglyceridemia; ? combined with serious primary diseases such as cardiovascular, liver, kidney and hematopoietic system; suspected mental patients; ? for Those who are allergic to the study drug or any excipients;

Outcomes

Primary Outcomes

Not specified

Similar Trials