Cataract Clinical Trial
Official title:
Pain Perception and Discomfort of Second Eye Cataract Surgery in Comparison With the First Eye in Correlation With Perioperative Stress
Purpose of this study is to find a correlation between agitation (stress) indicating parameters and the pain perception during second eye cataract surgery, compared to first eye cataract surgery.
Status | Recruiting |
Enrollment | 39 |
Est. completion date | January 1, 2021 |
Est. primary completion date | January 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years to 105 Years |
Eligibility |
Inclusion Criteria: - Age 21 and older - written informed consent prior to surgery - bilateral age-related cataract Exclusion Criteria: - deafness - allergy to topical anesthetic agents - severe anxiety and involuntary eye and head movements - conditions likely to require surgical therapy other than routine phacoemulsification (eg: traumatic and complicated cataracts) - in case of pregnancy (pregnancy test will be taken in women of reproductive age) |
Country | Name | City | State |
---|---|---|---|
Austria | Vienna Institute for Research in Ocular Surgery (VIROS) | Vienna |
Lead Sponsor | Collaborator |
---|---|
Prim. Prof. Dr. Oliver Findl, MBA |
Austria,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Perioperative agitation (stress) measurement | Perioperative stress will be measured using the BioLink Biofeedback device, which records an electrocardiogram, an electromyogram, skin conductance and respiratory rate. Changes in the different values show how stressed the patient was during the surgeries. | 12 months | |
Secondary | Assessment of pain perception | Pain perception of the patients will be assessed during the two cataract surgeries using an visual analogue scale, where 10 means highest pain and 1 is lowest pain. | 12 months |
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