- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04283708
Esthetic Outcome of Isolated Advancement Genioplasty With and Without Submental Liposuction in Treatment of Skeletal Chin Deficiency
February 21, 2020 updated by: Marwan Mohamed Atef Ahmed Lotfy, Cairo University
Measuring the Eshetic Difference Between Advancement Genioplasty With and Without Submental Liposuction in Treatment of Skeletal Chin Deficiency in Double Chin Patients
This study is to measure the eshetic outcome of of isolated advancement genioplasty with and without submental liposuction in treatment of skeletal chin deficiency in double chin patients
Study Overview
Detailed Description
Many methods used to treat skeletal chin deficiency in double chin patients, the aim of this study is to measure the advancement genioplasty with and without submental liposuction
Study Type
Interventional
Enrollment (Anticipated)
22
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: Mostafa Ibrahim Shindy, Phd
- Phone Number: 01121112222
- Email: M2shindy@hotmail.com
Study Contact Backup
- Name: Mohamed Khashaba, Phd
- Phone Number: 01227754765
Study Locations
-
-
-
Cairo, Egypt, 11553
- Marwan mohamed atef ahmed lotfy
-
Contact:
- Mostafa Ibrahim Shindy, Phd
- Phone Number: 01121112222
- Email: M2shindy@hotmail.com
-
Contact:
- Mohamed Khashaba, Phd
-
-
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 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- skeletal chin deficiency
- double chin patients
- Ages from 18 to 45
- systemic free
Exclusion Criteria:
- body mass index greater than 28
- ages greater than 45
- systemically diseased
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 |
---|---|
Experimental: Skeletal chin deficiency
Advancement genioplasty with submental liposuction
|
Advancement Genioplasty With Submental Liposuction
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
% of patient satisfaction
Time Frame: 6 months postoperative
|
scale of units/discrets
|
6 months postoperative
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Anticipated)
March 1, 2020
Primary Completion (Anticipated)
January 1, 2021
Study Completion (Anticipated)
March 1, 2021
Study Registration Dates
First Submitted
February 14, 2020
First Submitted That Met QC Criteria
February 21, 2020
First Posted (Actual)
February 25, 2020
Study Record Updates
Last Update Posted (Actual)
February 25, 2020
Last Update Submitted That Met QC Criteria
February 21, 2020
Last Verified
February 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Omfs337
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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