A study to develop a novel ophthalmic testing method in patients with cystinosis
- Conditions
- CystinosisD003554
- Registration Number
- JPRN-jRCTs031220490
- Lead Sponsor
- Yamamoto Yuuka
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 6
Patients with cystinosis who meet the following criteria
1) Patients with presence of corneal cystine crystal deposits assessed during ophthalmic examination
2) Patients who have ability to or intend to comply with the 4 times daily instillation regimen
3) Patients who are judged by the principal investigator or sub-investigator to be appropriate for inclusion in the study.
4) Patients who have given written consent to participate in the research in person.
5) Patients who are at least 18 years of age at the time consent is obtained
1) Patients who are obviously suffering from a serious acute disease
2) Patients with a history of hypersensitivity to the active ingredients or additives of the test drug
3) Pregnant or possibly pregnant or lactating women
4) Persons who are judged by the principal investigator to be inappropriate for inclusion in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method uminance waveform analysis (LWA) by using AS-OCT
- Secondary Outcome Measures
Name Time Method Photophobia rated by investigators<br>Photophobia rated by patients