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Clinical Trials/NCT02595125
NCT02595125
Completed
Not Applicable

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

Centre Hospitalier Universitaire de Saint Etienne1 site in 1 country60 target enrollmentFebruary 24, 2016
ConditionsContraception

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Contraception
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Enrollment
60
Locations
1
Primary Endpoint
Pain measured by Verbal Numeric Scale
Status
Completed
Last Updated
8 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
February 24, 2016
End Date
July 19, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Any major patient and consultant for IUD insertion : hormonal or copper
  • Signing of the information and consent form by the patient or, if under supervision by parents or guardian.
  • Patient affiliated with or entitled to a social security scheme
  • No contraindication for IUD insertion

Exclusion Criteria

  • Patient consultant for IUD insertion to side arms
  • Contraindications for installation.
  • Legal incapacity or limited legal capacity. Medical or psychological conditions not allowing the subject to understand the study and sign the consent
  • Refusal to sign the consent.

Outcomes

Primary Outcomes

Pain measured by Verbal Numeric Scale

Time Frame: intraoperative

Pain is score by Verbal Numeric Scale : 0-10 (0 = no pain; 10= pain as bad as can be)

Secondary Outcomes

  • Pain measured by Verbal Numeric Scale(day 7)
  • Number of analgesic intake(up to 7 days post-insertion)
  • Number of vagal discomfort(intraoperative)
  • Number of IUD-fond uterine distance >2 cm(intraoperative)
  • Number of emergency department visit for a IUD complication(up to 7 days)
  • Number of failure laying direct technique(intraoperative)
  • Number of expulsion of the IUD(intraoperative)
  • Number of expulsion of IUD(up to 7 days)

Study Sites (1)

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