Study to Assess Outcomes in Women Undergoing Either Hysteroscopic Sterilization (Essure®) or Laparoscopic Tubal Sterilization
Condition: Contraception · Sponsor: Bayer
About this study
This study is designed to assess post-procedural outcomes for women who chose to undergo either hysteroscopic sterilization (Essure®) or laparoscopic tubal sterilization, including: * Pelvic and/or lower abdominal pain * Abnormal uterine bleeding * Surgical intervention (including "insert removal" and hysterectomy) * Allergic, hypersensitivity, or autoimmune-like reactions
This description comes directly from the study's public registry record.
Talk to the study team
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Locations (57)
| New Horizons Women's Care | Chandler, Arizona, United States | — |
| Precision Trials, AZ, LLC | Phoenix, Arizona, United States | — |
| Visions Clinical Research - Tucson | Tucson, Arizona, United States | — |
| Eclipse Clinical Research | Tucson, Arizona, United States | — |
| Baptist Health Center for Clinical Research | Little Rock, Arkansas, United States | — |
| United Clinical Research | Huntington Beach, California, United States | — |
| Orange Coast Women's Medical Group - Laguna Hills Office | Laguna Hills, California, United States | — |
| Physicians Research Options, LLC | Lakewood, Colorado, United States | — |
| The Women's Health Group, P.C. | Thornton, Colorado, United States | — |
| M & O Clinical Research, LLC | Fort Lauderdale, Florida, United States | — |
| Altus Research | Lake Worth, Florida, United States | — |
| Universal Axon Clinical Research | Miami, Florida, United States | — |
+ 45 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT03127722