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Bandage Contact Lens in Post Operative Ptosis Patients

NCT03375879 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2018-04-23

No results posted yet for this study

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.

Conditions

  • Ptosis
  • Blepharoptosis

Interventions

DEVICE

Bandage contact lens

Bandage contact lens

Sponsors & Collaborators

  • Robert Adam

    collaborator UNKNOWN

  • Forough Farrokhyar

    collaborator UNKNOWN

  • Sivisan Suntheralingam

    collaborator UNKNOWN

  • St. Joseph's Healthcare Hamilton

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-02-21
Primary Completion
2018-12-01
Completion
2018-12-01
FDA Device
Yes

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03375879 on ClinicalTrials.gov