Last updated on January 2019

Study to Assess Outcomes in Women Undergoing Either Hysteroscopic Sterilization (Essure ) or Laparoscopic Tubal Sterilization

Brief description of 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

Clinical Study Identifier: NCT03127722

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Bayer Clinical Trials Contact

The Women's Health Group, P.C.
Thornton, CO United States
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Recruitment Status: Open

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