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A randomized, double-blind, placebo-controlled clinical study to assess the efficacy of oral doxycycline for recurrence prevention after hysteroscopic resection of multiple endometrial polyps in the reproductive age group

A randomized, double-blind, placebo-controlled clinical study to assess the efficacy of oral doxycycline for recurrence prevention after hysteroscopic resection of multiple endometrial polyps in the reproductive age group

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061961
Enrollment
Unknown
Registered
2022-07-13
Start date
2022-07-30
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

endometrial polyp

Interventions

Experimental group:Doxycycline
Control group:Placebo

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 20-45 years; 2. Multiple endometrial polyps were diagnosed under hysteroscopy; 3. Hysteroscopy conforms to the clinical manifestations of chronic endometritis and the pathology conforms to the diagnostic criteria of chronic endometritis; 4. Uterine shape and endometrial development are normal; 5. No doxycycline or pregnancy contraindications; 6. Did not receive antibiotic treatment such as doxycycline within 1 month before enrollment; 7. Have not participated in other clinical research, and after fully understanding all the risks and inconveniences brought by this trial, are willing to follow the trial arrangement and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Intrauterine adhesions or uterine deformities, or combined with uterine organic lesions; 2. Infertility caused by other reasons such as tubal factors; 3. Menorrhagia, anemia, irregular menstruation 4. Simple hyperplasia and above endometrial lesions 5. People with mental or consciousness disorders; 6. Combined with severe chronic diseases (heart, lung, liver, kidney dysfunction); 7. Pregnant or lactating women; 8. Malignant tumors; 9. Allergic to the test drug or unable to tolerate the test check; 10. Failure to complete follow-up visits on a regular basis.

Design outcomes

Primary

MeasureTime frame
Recurrence rate;Miscarriage rate;Differences in uterine cavity flora;Symptoms of abnormal uterine bleeding;

Secondary

MeasureTime frame
Clinical Pregnancy Rate;Live birth rate;

Countries

China

Contacts

Public ContactHuiying Zhang

Tianjin Medical University General Hospital

huiying_zhang2020@126.com+86 15900320106

Outcome results

None listed

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