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Effects of uterine flora and lifestyle on chronic endometritis and its mechanism

Effects of uterine flora and lifestyle on chronic endometritis and its mechanism

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100054313
Enrollment
Unknown
Registered
2021-12-13
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-11-14

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

Conditions

chronic endometritis (CE)

Interventions

Case group:None
Control group:None

Sponsors

The Second Affiliated Hospital of South China University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1. Case group inclusion criteria: (1) Subjects between the ages of 20 and 49; (2) Sign the informed consent; (3) Those who have no cognitive impairment, can understand the content of the questionnaire, and cooperate with biological specimen collection and follow-up; (4) No abnormality in pathological examination and leucorrhea examination, and the positive immunohistochemistry of endometrial tissue for CD138/CD38 was diagnosed as chronic endometritis; (5) No gynecological tumors or other malignant diseases such as uterine fibroids, adenomyosis, ovarian cancer and cervical cancer; (6) Non-menstrual period; (7) No history of diabetes, hypertension, hyperlipidemia, immune system diseases, sexually transmitted diseases, serious heart, brain, liver and other diseases; (8) No history of taking antibiotics, hormones, immunosuppressants or taking Mirena in the past month. 2. Inclusion criteria for the control group: (1) Subjects between the ages of 20 and 49; (2) Sign the informed consent; (3) Those who have no cognitive impairment, can understand the content of the questionnaire, and cooperate with the collection of biological specimens; (4) Immunohistochemical negative for CD138/CD38 in endometrial tissue and no abnormality in pathological examination and B-ultrasound examination; (5) No vaginitis, endometritis, uterine fibroids, adenomyosis, ovarian cancer and cervical cancer and other gynecological uterine inflammatory diseases, gynecological tumors or other malignant diseases; (6) Regular menstruation, currently in non-menstrual period, non-contraceptive period, no vaginal douching and no uterine cavity operation within six months; (7) No history of diabetes, hypertension, hyperlipidemia, immune system diseases, sexually transmitted diseases, serious heart, brain, liver and other diseases; (8) No history of taking antibiotics, hormones, immunosuppressants or taking Mirena in the past month.

Exclusion criteria

Exclusion criteria: Subjects with missing essential or important data.

Design outcomes

Primary

MeasureTime frame
inflammatory factors;microorganisms;blood routine examination;ESR;C-reactive protein;coagulation function ;six sex hormones;

Countries

China

Contacts

Public ContactGao Hong

The Second Affiliated Hospital of South China University

191661222@qq.com+86 15211827295

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026