Intrauterine Adhesions Clinical Trial
Official title:
Treatment of Intrauterine Adhesions and Its Distribution of Genital Tract Flora
This study aims to investigate the treatment of intrauterine adhesion and the factors influencing its prognosis.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | December 31, 2021 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 20 Years to 45 Years |
Eligibility |
Inclusion Criteria: Inclusion Criteria(experimental group and control group): - Pre-operative adhesion score was =5 - The prior menstrual cycle was regular, and the sex hormone was normal - Patients had fertility requirement - Male semen examination showed normal - There were no severe systemic diseases, and no contradictions to aspirin, estrogen and surgery Inclusion Criteria(healthy control group): - regular menstrual cycles,diagnostic hysteroscopy with endometrial biopsy and laparoscopy as part of their infertility diagnostic work-up prior to IVF, hysteroscopy and subsequent pathological results having shown no abnormality in the uterine cavities and abdominal cavity - the healthy women recruited had male partners who were infertile and diagnosed with defective sperm function,such as asthenozoospermia, oligoasthenozoospermia, severe oligoasthenozoospermia and azoospermia, defined according to guidelines published by the World Health Organization. Exclusion Criteria: - Pre-operative adhesion score was <5 - Prior menstrual cycle was irregular and sex hormone was abnormal, or patients had endocrine factors that caused amenorrhea, menstrual reduction and infertility - Patients had no fertility requirement - Patients(experimental group and control group) had male factor infertility - Patients had contradictions to estrogen and aspirin such as cancers (breast cancer and endometrial cancer), thrombotic diseases, allergy to antipyretic analgesics, severe liver injury, hypoprothrombinemia, vitamin K deficiency, hemophilia, thrombocytopenia, gastric or duodenal ulcer and asthma. - refuse Endometrial biopsy - Vaginal discharge abnormal, or suspected vaginitis or pelvic inflammatory disease, or using antibiotics. |
Country | Name | City | State |
---|---|---|---|
China | Guangzhou | Guangdong | Guangzhou, Guangdong |
Lead Sponsor | Collaborator |
---|---|
First Affiliated Hospital, Sun Yat-Sen University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Endometrial Thickness of All Participants in the Mid Menstrual Measured by Color Doppler Ultrasound | 1 year | ||
Secondary | Menstruation Pattern(Improvement or No Significant Change) of All Participants | A method similar to visual analogue scale(VAS) was employed for the evaluation of post-operative menstruation with 0 as amenorrhea and 100 as normal menstruation. | 1 year | |
Secondary | Reduction of American Fertility Society adhesion score at Second-look | The severity and extent of intrauterine adhesions were scored according to a classification system recommended by the American Fertility Society (AFS) (1988 version) [7]. A score of 1-4 was considered to represent mild adhesions, a score of 5-8 was considered to represent moderate adhesions and a score of 9-12 represented severe adhesions. | one year | |
Secondary | Number of Participants With Pregnancy after operation | two years | ||
Secondary | Differences in distribution of reproductive tract bacteria between patients are before and after operation | one year | ||
Secondary | Differences in distribution of reproductive tract bacteria between healthy control group and intrauterine adhesion patients | one year |
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