Clinical Trials Logo

Clinical Trial Summary

In this non-interventional study we investigate the nulliparous women individual evaluation of the insertion procedure of LNG-IUD and the follow-up period of 3 months post insertion.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00798980
Study type Observational
Source Bayer
Contact
Status Completed
Phase N/A
Start date February 2007
Completion date November 2009

See also
  Status Clinical Trial Phase
Completed NCT04321642 - The Effect of Entonox on Stages of Labor in Nulliparous Women N/A
Not yet recruiting NCT02396563 - Effect of Epidural Analgesia on the Length of Labor and Delivery and Fetal Outcomes N/A
Not yet recruiting NCT05696574 - Oral and Vaginal Misoprostol for Induction of Labor in Nulliparous Pregnant Women N/A
Recruiting NCT05568745 - Balloon + Oxytocin Versus Oral Misoprostol to Induce Labor in Case of PROM (RUBAPRO2) Phase 4
Withdrawn NCT03934918 - Outpatient Cervical Preparation to Reduce Induction Duration in NTSV Women N/A