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
| Type | Name | Description |
|---|---|---|
| DEVICE | IUD | copper 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.