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Clinical Trial Summary

To investigate whether vaginal dinoprostone administered before the levonorgestrel-releasing intrauterine system(IUs) insertion reduces failed insertions, insertion-related complications, and pain in Women With no Previous Vaginal Delivery.


Clinical Trial Description

Long-acting reversible contraception methods are highly effective methods for reduction of the unplanned pregnancy rate worldwide. The intrauterine device is a single procedure that provides reliable, effective and long term contraception for many women. However, the insertion procedure can be associated with a troublesome degree of pain that prevent some women from choosing its use. Different interventions have been described to decrease pain perception during intrauterine device insertion with no agreement on an effective one. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04045548
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase Phase 4
Start date August 10, 2019
Completion date January 5, 2020

See also
  Status Clinical Trial Phase
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