Trial · NCT02660151
Study of Using the Hyper-CL™ Lens (Hyper Osmotic Contact Lens) in Subjects Suffering From Corneal Edema
NCT02660151, Not applicable, Completed, Eye-yon Medical
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Study of Using the Hyper-CL™ Lens (Hyper Osmotic Contact Lens) in Subjects Suffering From Corneal Edema. Trials, record NCT02660151. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02660151
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Study of Using the Hyper-CL™ Lens (Hyper Osmotic Contact Lens) in Subjects Suffering From Corneal Edema
- NCT number
- NCT02660151
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 68 participants, actual
- Lead sponsor
- Eye-yon Medical
- Conditions
- CORNEAL EDEMA
- Interventions
- Hyper-CL™ lens, Regular soft contact lens, Salt solution
- First posted
- 2016-01-21
- Last updated
- 2019-05-21
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | frequency and severity of all treatment-related adverse events | Up to 28 days (or 21 days if wash out is not needed). | |
| Primary | Percent of subjects with corneal thickness decrease of at least 8% and or visual acuity improvement of at least 1 line following treatment with the Hyper-CL™ lens + salt solution | Up to 28 days (or 21 days if wash out is not needed). | assess by physiological parameter |
| Secondary | Percent of subjects with corneal thickness decrease of at least 8%. | Up to 28 days (or 21 days if wash out is not needed). | assess by physiological parameter |
| Secondary | Percent of subjects with visual acuity improvement of at least 1 line | Up to 28 days (or 21 days if wash out is not needed). | assess by physiological parameter |
| Secondary | Corneal thickness decrease | Up to 28 days (or 21 days if wash out is not needed). | assess by physiological parameter |
| Secondary | change in Measurement Best Corrected Distance Visual Acuity (BCDVA) | Up to 28 days (or 21 days if wash out is not needed). | |
| Secondary | change in Subject comfort questionnaire | Up to 28 days (or 21 days if wash out is not needed). |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 33014443 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02660151
GET https://conductscience.org/api/trials/v1/NCT02660151/registered