ISRCTN31552904Completed未知
Determination of corneal biomechanical properties in-vivo using a contact device: a single-arm, observational study
niversity of Liverpool (UK)0 sites70 target enrollmentStarted: July 23, 2014Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 70
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1. At least 18 years of age
- •2. Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant
- •3. Normal ophthalmic findings, other than high IOP
- •4. Astigmatism <2D
- •5. Potential to complete the study and comply with appropriate instructions
- •6. Signature on the informed consent form
Exclusion Criteria
- •1. Corneal pathology or previous intra- or extra-ocular surgery, including refractive surgery (e.g., radial keratotomy, photorefractive keratotomy, LASIK, intracorneal ring), retinal surgery (e.g., buckle, photocoagulation), or implantation of a primary or secondary intraocular lens
- •2. Contact lens wearing within 3 days (rigid contact lenses) or 1 day (soft contact lenses) prior to study day
- •3. Inability to fully understand the ?informed consent?
- •4. Participants who are diabetic
Investigators
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