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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04636372
Other study ID # LXY-meibomian gland
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date January 31, 2021

Study information

Verified date September 2020
Source Wenzhou Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

200 participants at Eye Hospital of Wenzhou Medical University during September, 2020 to November, 2020 will be enrolled in this study. The meibomian gland related therapy are pulsed light therapy and meibomian gland hot compress massage.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 31, 2021
Est. primary completion date January 31, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Previously untreated patients with xerophthalmia Exclusion Criteria: - No history of ocular surgery and trauma - Any eye diseases except xerophthalmia - No treated for xerophthalmia before - Successful completion of follow-ups

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Intense pulsed light therapy
Patients with xerophthalmia were treated with intense pulsed light of meibomian gland.
Other:
Hot compress massage
Patients with xerophthalmia were treated with hot compress massage of meibomian gland.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yune Zhao

Outcome

Type Measure Description Time frame Safety issue
Primary The length of meibomian glands after the treatment. Length in millimeters. up to 2 months
Primary The area of meibomian glands after the treatment. Area in millimeters^2. up to 2 months
Primary The percentage of meibomian glands after the treatment. Percentage of meibomian glands in %(area of meibomian glands (mm^2) and area of palpebral conjunctiva (mm^2) will be combined to report percentage of meibomian glands in %) are used to assess this outcome measure. up to 2 months
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