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Clinical Trial Summary

Aim of this study is to evaluate the effect of VR on the patients overall experience during the IUD insertion procedure.


Clinical Trial Description

A single center, investigator initiated randomized controlled clinical trial. 200 women to be recruited, 100 in the intervention group and 100 in the control group. The control group will receive the usual treatment (without specific pain management) and the intervention group will receive the usual treatment with VR support. Endpoints are: - Objective: successful procedure, need for general anesthesia, presence of syncope and/or vomitus - Subjective: Pain, procedural cooperation, the degree of difficulty encountered by the physician in performing the treatment, ability to complete VR procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04389021
Study type Interventional
Source Universitaire Ziekenhuizen Leuven
Contact
Status Completed
Phase N/A
Start date March 1, 2020
Completion date January 1, 2021

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