- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05682001
The Molecular Pathogenesis Study of Cataract
January 3, 2023 updated by: Jin Yang, Eye & ENT Hospital of Fudan University
To study the molecular pathogenesis of cataract and explore possible treatments,anterior lens capsules were collected from cataract patients
Study Overview
Status
Recruiting
Conditions
Detailed Description
Anterior lens capsules were collected from the patients with DC and ARC, and transparent crystals of cadaveric eyes.
M6A epitranscriptomic microarray was performed to investigate the altered m6A modifications and determine the differentially expressed mRNAs.
The potential role of dysregulated m6A modification levels was predicted through Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses.
Real-time polymerase chain reaction was performed to identify the dysregulated expression of RNA methyltransferases, demethylases, and readers.
Study Type
Observational
Enrollment (Anticipated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Lei Cai, MD
- Phone Number: 13816956828
- Email: clyc0318@126.com
Study Locations
-
-
Shanghai
-
Shanghai, Shanghai, China, 200031
- Recruiting
- Eye & ENT Hospital of Fudan University
-
Contact:
- Jin Yang, PhD
- Phone Number: 13671632525
- Email: jin_er76@hotmail.com
-
Principal Investigator:
- Lei Cai, MD
-
Principal Investigator:
- Dongmei Ma, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Anterior lens capsule tissues from cataract patients with diabetes mellitus more than 10 years, patients with age related cataract, and transparent crystals of cadaveric eyes.
Description
Inclusion Criteria:
- diabetic cataract
- underwent cataract surgery
Exclusion Criteria:
- Combined with other eye diseases
- underwent other eye surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
|
DC group
Anterior lens capsule tissues from DC patients
|
|
ARC group
Anterior lens capsule tissues from ARC patients
|
|
NC group
anterior lens capsules collected from three age-matched transparent crystals of cadaveric eyes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
m6A modification of mRNAs
Time Frame: 1 month
|
Epitranscriptomic microarray analysis reveals the differential m6A modification of mRNAs in DC samples
|
1 month
|
|
expression level of mRNAs
Time Frame: 1 month
|
the m6A microarray analyses provide data for mRNA expression levels
|
1 month
|
|
levels of methylated mRNA
Time Frame: 1 month
|
in vitro validation of the diverse expression levels of methylated mRNA
|
1 month
|
|
levels of RNA methyltransferase
Time Frame: 1 month
|
in vitro validation of the diverse expression levels of RNA methyltransferase
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Jin Yang, PhD, Eye & ENT Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2022
Primary Completion (Anticipated)
December 1, 2023
Study Completion (Anticipated)
December 30, 2025
Study Registration Dates
First Submitted
December 6, 2022
First Submitted That Met QC Criteria
January 3, 2023
First Posted (Actual)
January 12, 2023
Study Record Updates
Last Update Posted (Actual)
January 12, 2023
Last Update Submitted That Met QC Criteria
January 3, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CMP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.