- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04861454
Brassiere Brow Suture and Internal Browpexy
November 16, 2023 updated by: Tarek Roshdy mohamed Mahgoub ELhamaky, Benha University
Brassiere Brow Suture and Internal Browpexy as Disjunctive Upper Eyelid Blepharoplasty
Brow ptosis is a common problem.
internal browbexy and brassier suture are common surgical approach
Study Overview
Status
Recruiting
Conditions
Detailed Description
upper eye transcutaneous blepharoplasty then combined browbexy and brassier suture are done
Study Type
Observational
Enrollment (Estimated)
30
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: TAREK R ELHAMAKY, MD
- Phone Number: +971 503207889
- Email: dr_thamakyy@yahoo.com
Study Contact Backup
- Name: TAREK ELHAMAKY
Study Locations
-
-
-
Abu Dhabi, United Arab Emirates, 46266
- Recruiting
- INMC
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
At least 18 years with dermatochalasis
Description
Inclusion Criteria:
- brow ptosis and dermatochalasis
Exclusion Criteria:
- eyelid diseases and previous 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
Cohorts and Interventions
Group / Cohort |
---|
surgical
internal browbexy and brassier suture were done after blepharoplasty
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
global aesthetic scale
Time Frame: 1 year
|
calculate scale score from score 1 exceptional improvement to 5 worsening patient
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: tarek elhamaky, MD, benha faculty of medicine
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 10, 2021
Primary Completion (Estimated)
July 10, 2024
Study Completion (Estimated)
July 20, 2024
Study Registration Dates
First Submitted
April 19, 2021
First Submitted That Met QC Criteria
April 25, 2021
First Posted (Actual)
April 27, 2021
Study Record Updates
Last Update Posted (Estimated)
November 17, 2023
Last Update Submitted That Met QC Criteria
November 16, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hamaky10
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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