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NCT02527278

Retrospective Claims Analysis of Hysterectomy After Sterilization

Completed Last updated 21 March 2017
What this trial tests

trial testing Laparoscopic tubal ligation in Contraception in 19,317 participants. Completed in 9 February 2016.

Timeline
30 July 2015
Primary endpoint
9 February 2016
9 February 2016

Quick facts

Lead sponsorBayer
StatusCompleted
Study typeOBSERVATIONAL
Enrollment19,317
Start date30 July 2015
Primary completion9 February 2016
Estimated completion9 February 2016
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Bayer — full company profile →

Who can join

Adults 18 to 49, female only, with Contraception. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The research questions are: 1. What is the proportion of women undergoing hysterectomy after hysteroscopic sterilization or laparoscopic tubal ligation? 2. What is the proportion of women undergoing salpingectomy, salpingostomy, or hysteroscopy after hysteroscopic sterilization or laparoscopic tubal ligation? 3. What is the proportion of women who have a diagnosis of pelvic pain after hysteroscopic sterilization or laparoscopic tubal ligation?

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Contraception

Currently open trials in the same condition.

Other Bayer trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02527278.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing