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ENROLLING BY INVITATION
NCT07624929
NA

The Use of Immersive Virtual Reality as a Method of Treating Anxiety and Procedural Pain During Endovenous Laser Ablation (EVLA) of Lower Varicose Veins Under Tumescent Anesthesia

Sponsor: Bydgoszcz University of Science and Technology

View on ClinicalTrials.gov

Summary

This is a prospective, single-arm, pre-post interventional study designed to evaluate the feasibility, safety, and impact of immersive virtual reality (VR) as an adjunct to tumescent local anesthesia during endovenous laser ablation (EVLA) for varicose veins / chronic venous insufficiency. All eligible and consenting participants will receive the same intervention (immersive VR during the entire EVLA procedure). There is no randomization, no control group, and no allocation to different arms. Each participant serves as their own control through before-and-after comparisons

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-06-10

Completion Date

2028-09-10

Last Updated

2026-06-09

Healthy Volunteers

No

Interventions

DEVICE

VR (VR-Control)

Immersive Virtual reality

Locations (1)

Bydgoszcz Univ of Science and Technology

Bydgoszcz, Poland