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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03907358
Other study ID # Shanghai1st-cataract-001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 7, 2016
Est. completion date June 30, 2020

Study information

Verified date April 2019
Source Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Contact Haidong Zou
Phone 86-21-63240090
Email zouhaidong@hotmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To study the pathological mechanism of cataract by genomics, transcriptomics, and proteomics.


Description:

Tissue samples and aqueous humor samples will be collected from each individual patients by cataract surgery. After sample treatment, different techniques will be applied for analysis. And bioinformatics approach is applied for data treatment and analysis.The data of genomics, transcriptomics, and proteomics will be analyzed for study of pathological mechanism of cataract.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date June 30, 2020
Est. primary completion date December 30, 2019
Accepts healthy volunteers No
Gender All
Age group 5 Years to 94 Years
Eligibility Inclusion Criteria:

- Patients with the explicit diagnosis of cataract (including senile cataract, congenital cataract, complicated cataract, metabolic cataract, traumatic cataract, etc.) in the operated eye are willing to undergo cataract surgery.

Exclusion Criteria:

- Patients whose cataracts need not be operated

- Patients with any contraindications to cataract surgery

- Patients are unwilling to undergo cataract surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
phacoemulsification


Locations

Country Name City State
China Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiao Tong University Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Characterization of miRNA in micro-scale human aqueous humor method development for miRNA detection in aqueous humor 12 month
Primary Favored amplification recovery via protection-chromatin immunoprecipitation-Seq of human eye tissue samples low-cell-number epigenome profiling for study of cataract 24 month
Primary Study of cataract by genomics, transcriptomics, and proteomics approaches detect histone H3 lysine 4 trimethylation (H3K4me3) of aqueous humor of cataract patients by genomics, transcriptomics, and proteomics methods 36 month
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