CompletedNot Applicable

Clinical Efficacy of Virtual Reality During Office Hysteroscopy and Endometrial Biopsy in Subfertility

Belgium216 participantsStarted 2020-09-10

Plain-language summary

This study is a comparison between the current standard practice of performing a diagnostic hysteroscopy and a relatively recently developed technology that is added to the standard diagnostic hysteroscopy. The aim of the study is to find out whether this newer technology has an advantage for the patient, in the form of anxiety and pain reduction.

Who can participate

Age range18 Years – 48 Years

SexFEMALE

See this in plain English?

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Exclusion criteria

✕. Hearing impairments and blindness
✕. Motion sickness
✕. Any known anatomical characteristics that may make performing the office procedure impossible.
✕. The unwillingness of the patient to undergo an office hysteroscopy
✕. Denial or withdrawal of informed consent

What they're measuring

Change in pain experience as assessed using visual analog scale

Timeframe: 1/ baseline pre-procedure 2/ immediately after the procedure (1+2= day of office hysteroscopy) and 3/ 1 week after the procedure

Trial details

NCT IDNCT04438759

SponsorUniversitair Ziekenhuis Brussel

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-08-31

View on ClinicalTrials.gov More Infertility, Female trials