- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05290896
Correlations Between Lens Star and Phacoemulsification.
March 12, 2022 updated by: Ahmed Abdelshafy, Benha University
Correlations Between Lens Star Parameters and Phacoemulsification in Clinical Practice.
To assess correlations between lens star biometry parameters and phacoemulsification in clinical practice.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
To analyze possible correlations between lens star biometry parameters and phacoemulsification in mild to moderate senile cataract.
Study Type
Interventional
Enrollment (Anticipated)
100
Phase
- Not Applicable
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: Ahmed Abdelshafy, MD
- Phone Number: 01222328766
- Email: ahmad4lg@gmail.com
Study Contact Backup
- Name: Marwa Abdelshafy, MD
- Phone Number: 01222328766
- Email: drmarwatabl2012@gmail.com
Study Locations
-
-
QA
-
Banhā, QA, Egypt, 13511
- Recruiting
- Ahmed Abdelshafy
-
Contact:
- Ahmed Abdelshafy
- Phone Number: 01222328766
- Email: ahmad4lg@gmail.com
-
Contact:
- Email: ahmad4lg@gmail.com
-
Principal Investigator:
- Ahmed Abdelshafy, 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
36 years to 76 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients that will undergone phacoemulsification for their mild to moderate senile cataracts.
Exclusion Criteria:
- congenital and developmental cataract.
- cases with congenital lens anomalies as ectopia lentis and spheophakia.
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
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Lens star biometry
Biometry done prior to phacoemulsification
|
Phacoemulsification for senile cataract.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation between parameters measured by lens star.
Time Frame: Immediately before phacoemulsification surgery
|
Anterior chamber depth, lens, axial length, keratometry readings and age of the patients.
|
Immediately before phacoemulsification surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ahmed A Abdelshafy, MD, Benha University
- Study Director: Marwa A Abdelshafy, MD, Benha University
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)
February 20, 2022
Primary Completion (Anticipated)
August 30, 2022
Study Completion (Anticipated)
September 15, 2022
Study Registration Dates
First Submitted
March 12, 2022
First Submitted That Met QC Criteria
March 12, 2022
First Posted (Actual)
March 22, 2022
Study Record Updates
Last Update Posted (Actual)
March 22, 2022
Last Update Submitted That Met QC Criteria
March 12, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Rc-3-29
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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.
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