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Comparison of three methods for preventing re-adhesion after hysteroscopic intrauterine adhesion separation

Comparison of three methods for preventing re-adhesion after hysteroscopic intrauterine adhesion separation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046945
Enrollment
Unknown
Registered
2021-05-31
Start date
2016-01-01
Completion date
Unknown
Last updated
2022-01-10

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

Conditions

Intrauterine adhesions

Interventions

Group A (IUD):intrauterdevice (IUD) implantation
Group B (Foley1w+IUD):IUD implantation one week after intrauterine balloon placement
Group C (Foley1M+IUD):IUD implantation one month after intrauterine balloon placement

Sponsors

Nantong Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. People aged 20 to 35 years with reduced menstrual volume or amenorrhea symptoms; 2. Primary treatment of patients with medium and severe adhesion by AFS score; 3. Birth requirements, and intrauterine adhesion is the only infertility factor in patients; 4. No taboos for hormones or antibiotics; 5. Good compliance, willing to cooperate with the diagnosis and treatment plan of patients.

Exclusion criteria

Exclusion criteria: 1. Having a severe endosurgical disease affects the analysis outcomes; 2. Sex hormones suggest people with declining ovarian function; 3. Genital tract inflammation, tuberculosis, tumors, and malformations.

Design outcomes

Primary

MeasureTime frame
AFS score;

Secondary

MeasureTime frame
endometrial thickness;pregnancy rate;

Countries

China

Contacts

Public ContactYiqian Ding

Nantong Maternal and Child Health Hospital

1910677654@qq.com+86 15862716008

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026