Virtual Reality During Conization of Cervix Uterus Under Local Anesthesia

  • STATUS
    Recruiting
  • End date
    Mar 13, 2024
  • participants needed
    100
  • sponsor
    Tel-Aviv Sourasky Medical Center
Updated on 13 June 2022
anesthesia
cone biopsy

Summary

To evaluate the effectiveness of virtual reality glasses as a distraction technique in the management of acute pain and anxiety during conization of cervix uterus under local anesthesia

Description

A prospective, open-label, randomized control trial in a tertiary university affiliated medical center between March 2021 to March 2023. Overall, 100 women referred for conization of cervix due to cervical dysplasia will be randomly allocated to undergo conization either with the use of virtual reality glasses (study group) or with standard treatment (control group). The primary outcome measures will include self-reported pain, anxiety scores, and vital signs as an indirect measurement of pain and anxiety, including pulse rate (PR) and respiratory rate (RR). Pain and anxiety outcomes will be measured as numeric rating scores.

Details
Condition Dysplasia, Cervix
Treatment SootheVR: AppliedVR, Los Angeles, California a head-mounted display
Clinical Study IdentifierNCT04742543
SponsorTel-Aviv Sourasky Medical Center
Last Modified on13 June 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients over 18 years referred for conization of cervix due to cervical
dysplasia

Exclusion Criteria

patients under 18 years
pregnant women
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