RELIEF OF PSYCHOEMOTIONAL STRESS USING XENON SEDATION
Recruiting
Early Phase 1
Interventional Study
Psychological Stress
Anesthesia
Anxiety
Xenon
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 45
- Sex
- Any
- Trial phase
- Early Phase 1
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 140 (estimated)
- Sponsor
- The S.N. Fyodorov Eye Microsurgery State Institution · Government
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About This Trial
The goal of this clinical trial is to propose for implementation and evaluate the effectiveness of xenon sedation for the relief of psychoemotional stress disorder before the operation of refractive laser vision correction patients with high anxiety and stress instability who underwent xenon analgosedation before refractive laser vision correction. The main question\[s\] it aims to answer are:
1.…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* upcoming operation ReLEx® SMILE;
* high anxiety and stress instability (Spielberger-Khanin test of 46 points or more);
* signed informed consent to participate in the study.
Exclusion Criteria:
\- concomitant somatic diseases in the decompensation stage.
Contacts