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The study of preventing complications of performance place and remove contraceptive devices

The study of preventing complications of performance place and remove contraceptive devices

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OO-12002603
Enrollment
Unknown
Registered
2012-10-22
Start date
2007-12-22
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

Iud complications

Interventions

Total:intrauterine device

Sponsors

National Research Institute for Family Planning
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 76 Years

Inclusion criteria

Inclusion criteria: Women who intend to place or remove the IUD, and implants, without performance contraindications.

Exclusion criteria

Exclusion criteria: Any one with contraindications of this performance.

Design outcomes

Primary

MeasureTime frame
perforation of uterus;organ injury;bleeding;anaphylaxis;pain;Cardio-cerebral syndrome;infection;IUD ectopia;—

Countries

China

Contacts

Public ContactZou Yan
zyljlyh@yahoo.com.cn+86 010 62173456

Outcome results

None listed

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