Clinical Trials Directory

Trials / Completed

CompletedNCT02532361

Proportion of Hysterectomy After Female Sterilization

A Retrospective Analysis to Describe the Proportion of Hysterectomy After Female Sterilization With Hysteroscopic Device or Tubal Ligation Using Intermountain Healthcare Database in the US

Status
Completed
Phase
Study type
Observational
Enrollment
10,578 (actual)
Sponsor
Bayer · Industry
Sex
Female
Age
18 Years – 49 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to describe the proportion of hysterectomy in patients that had undergone sterilization through hysteroscopic device placement and the patients that had undergone sterilization through tubal ligation.

Conditions

Interventions

TypeNameDescription
DEVICEHysteroscopic device placement including Essure (ESS305, BAY1454032)Essure is a permanent, minimally invasive, non-hormonal implantable device used for contraception and Adiana sterilization method is a combination of controlled thermal damage to the lining of the fallopian tube followed by insertion of a non-absorbable biocompatible silicone elastomer matrix within the tubal lumen
PROCEDURETubal ligationTubal ligation or tubectomy is a surgical procedure for sterilization in which a woman's fallopian tubes are clamped and blocked, or severed and sealed, either method of which prevents eggs from reaching the uterus for implantation

Timeline

Start date
2015-08-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2015-08-25
Last updated
2016-12-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02532361. Inclusion in this directory is not an endorsement.