NCT03754556View on ClinicalTrials.gov

Study on Medical Records of Women Using an Intrauterine Device (IUD) to Analyze the Risks That the IUD Will be Expelled or Perforates the Womb in Relation to Breastfeeding, the Point in Time When the IUD Was Inserted After Childbirth and in Relation to Different Types of IUDs

CompletedOBSERVATIONAL
Enrollment

326,658

Participants

Timeline

Start Date

December 3, 2018

Primary Completion Date

November 29, 2019

Study Completion Date

November 29, 2019

Conditions
Intrauterine Devices
Interventions
DEVICE

Intrauterine device

Intrauterine devices, e.g. BAY86-5028 (Mirena, Skyla, Kyleena), Liletta and ParaGard

Trial Locations (4)

46202

Regenstrief Institute, Indianapolis

91101

Kaiser Permanente Southern California, Pasadena

94612

Kaiser Permanente Northern California, Oakland

98101

Kaiser Permanente Washington, Seattle

Sponsors

Lead Sponsor

Bayer
All Listed Sponsors
lead

Bayer

INDUSTRY

NCT03754556 - Study on Medical Records of Women Using an Intrauterine Device (IUD) to Analyze the Risks That the IUD Will be Expelled or Perforates the Womb in Relation to Breastfeeding, the Point in Time When the IUD Was Inserted After Childbirth and in Relation to Different Types of IUDs | Biotech Hunter | Biotech Hunter