Home
Search
Study Topics
Glossary
|
|
|
|
|
|
Sponsored by: |
FORSIGHT Vision3 |
---|---|
Information provided by: | FORSIGHT Vision3 |
ClinicalTrials.gov Identifier: | NCT00691925 |
Using Contact lens following refractive procedure to reduce pain.
Condition |
---|
Pain |
Study Type: | Observational |
Study Design: | Cohort, Prospective |
Official Title: | Contact Lens for Mitigating Pain Following Refractive Procedure |
Estimated Enrollment: | 10 |
Study Start Date: | June 2008 |
Estimated Study Completion Date: | August 2008 |
Estimated Primary Completion Date: | July 2008 (Final data collection date for primary outcome measure) |
Groups/Cohorts |
---|
1
bilateral post refractive surgery subject
|
Patients at day 1 following the procedure will be treated with a contact lens and assessed for pain at 1,2,4 hours and 1,3,5 days.
prospective comparative study
Ages Eligible for Study: | 18 Years to 60 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
at least 10 subjects following refractive surgery
Inclusion Criteria:
Exclusion Criteria:
Contact: Osnat Ehrman, MSc | 952-334-5797 | osnat.ehrman@gmail.com |
Israel | |
Sorasky Medical Center | Recruiting |
Tel Aviv, Israel | |
Contact: David Verssano, MD | |
Principal Investigator: David Verssano, MD | |
Sub-Investigator: Moshe Lazar, MD | |
Sub-Investigator: Yossi Yatziv, MD |
Principal Investigator: | David Verssano, MD | Sorasky Medical Center |
Responsible Party: | FORSIGHT ( Osnat Ehrman ) |
Study ID Numbers: | 0164 |
Study First Received: | June 4, 2008 |
Last Updated: | August 22, 2008 |
ClinicalTrials.gov Identifier: | NCT00691925 |
Health Authority: | Israel: Ministry of Health |
refractive surgery |
Pain |