Physiological Upper Eyelid Laxity

Eyelid Laxity Clinical Trial

— LAX  

Official title:

Physiological Upper Eyelid Laxity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03439644
• Other study ID #: LAX
• Status: Completed
• Phase: N/A
• First received: February 8, 2018
• Last updated: February 19, 2018
• Start date: October 25, 2017
• Est. completion date: November 27, 2017

Study information

• Verified date: February 2018
• Source: Poitiers University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, single-center study in normal subjects aged 20 to 89 years.

The objective was to describe upper eyelid laxity by age group (20/29 years old, 30/39 years old, 40/49 years old, 50/59 years old, 60/69 years old, 70/79 years old and 80/89 years old) measured with the method of McNab and studying it according to her customary side of sleep. In addition, we evaluated a method for measuring tarsal laxity.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 280
• Est. completion date: November 27, 2017
• Est. primary completion date: November 27, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 89 Years

Eligibility

Inclusion Criteria:

• 20 to 89 years

• be free

• be able to give informed consent

Exclusion Criteria:

• History of facial paralysis, upper palpebral trauma or palpebral surgery

• History of sleep apnea syndrome

• Impossibility to give consent

• Pregnant or lactating women

• Persons enjoying enhanced protection and persons deprived of their liberty by a judicial or administrative decision

Related Conditions & MeSH terms

• Eyelid Laxity

Intervention

Other:
• Measurement of the upper eyelid laxity
Measurement using a soft slider of the distance between our 2 marks The difference obtained between the measurement and the initial 10 millimeters corresponds to the tarsal laxity.

Locations

Country	Name	City	State
France	CHU DE Poitiers	Poitiers

Sponsors (1)

Lead Sponsor	Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evolution of upper eyelid laxity	Comparison of upper right and left palpebral laxity values in millimeters between different age groups	10 minutes