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Bandage Contact Lens in Post Operative Ptosis Patients

Blepharoptosis Clinical Trial

Official title:
The Role of Bandage Contact Lens in Post-operative Patients Undergoing Fasanella Servat Ptosis Repair

Clinical Trial Summary

This study is being conducted to determine whether the use of bandage contact lens after ptosis surgery provides any benefits for the patient or is unnecessary.

Clinical Trial Description

This study is being conducted to determine whether the use of bandage contact lens after ptosis surgery provides any benefits for the patient or is unnecessary. The investigators hope to show through questionnaires based on the patient's experience after their surgery to see if the bandage contact lens has provided any benefit for the patient. This is a randomized control trial in which patients undergoing bilateral ptosis surgery (Fasanella servat procedure) will have one of their eyes randomized to receive a bandage contact lens after surgery while the other eye will not receive anything.In this randomized control trial, patients requiring surgery with bilateral ptosis will have one eye randomized to receive a bandage contact lens whereas the other eye will not after their surgery. Follow up will occur in one week where the outcomes will be obtained through questionnaires. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03375879
Study type Interventional
Source St. Joseph's Healthcare Hamilton
Contact John Harvey, M.D.
Phone 905-522 1155
Email johntharvey@gmail.com
Status Recruiting
Phase N/A
Start date February 21, 2018
Completion date December 1, 2018
View Details
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