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Clinic observation of levonorgestrel releasing intrauterine system inserted in different periods

Clinic observation of levonorgestrel releasing intrauterine system inserted in different periods

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-16007752
Enrollment
Unknown
Registered
2016-01-13
Start date
2016-02-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

the effects of mirena

Interventions

inserting immediately after artificial abortion:none
inserting during menstrual period:none
inserting after menstruation:none
after curettage after menstruation:none

Sponsors

Hubei Women & Children Healthcare Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: women who underwent voluntary pregnancy termination and preferred levonorgestrel releasing intrauterine system insertion as a contraceptive method after counseling were enrolled

Exclusion criteria

Exclusion criteria: 1. any acute diseases; 2. the gynecological examination and assistant examination is unnormal.

Design outcomes

Primary

MeasureTime frame
removal rate;continuity rate;conception rate;amenorrhea rate;amenorrhea rate;spotting rate;oligomenorrhea rate;menorrhagia rate;—

Countries

China

Contacts

Public ContactTongfu Feng
ftfsunny@163.com+86 18986123645

Outcome results

None listed

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