Clinical Trials Directory

Trials / Completed

CompletedNCT02595125

Study Assessing the Reduction of Pain Felt During Installation Intra- Uterine Device by Direct Technique

Comparative Study, Prospective, Randomized , Assessing the Reduction of Pain Felt During Installation Intra- Uterine Device by Direct Technique. A Monocentric Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Centre Hospitalier Universitaire de Saint Etienne · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Intrauterine devices (IUDs) are contraceptive methods of long-acting (from 3 to 10 years depending on the model) and among the most effective. However, there are many obstacles to the use of IUDs including pain felt by patients during installation. Several medical means were studied without evidence of their efficacy in pain related to IUD insertion. In order to remove this brake, it's important to find another way to act against this pain. The direct technique is one of the techniques described by health professionals. It seems trusted by its users as a more reliable technique but also less painful for patients. However, there is no study available on its evaluation. The aim of this study is to investigate the interest of the direct technique in reducing the pain experienced by patients during installation.

Conditions

Interventions

TypeNameDescription
DEVICEIUDcopper IUD or levonogestrel IUD insert by the conventional technique or by direct technique

Timeline

Start date
2016-02-24
Primary completion
2017-07-12
Completion
2017-07-19
First posted
2015-11-03
Last updated
2018-01-29

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02595125. Inclusion in this directory is not an endorsement.