NCT06344689

Brief Summary

The main purpose of this study is to verify and compare the treatment effects of scarred ectropion surgery, perform statistical descriptions, compare patients undergoing tarsal strip and skin flap procedures with those undergoing simple skin flap treatment, and compare their pre- and post-operative Ectropion Grading Scale (EGS) and subjective and objective symptom changes. Secondary Objective: To observe the incidence and resolution of complications after lower eyelid ectropion surgery. Compare postoperative effects among patients of different ages undergoing the same surgery.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 12, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2024

Completed
28 days until next milestone

First Submitted

Initial submission to the registry

March 27, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 27, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 3, 2024

Completed
Last Updated

April 3, 2024

Status Verified

April 1, 2024

Enrollment Period

3 months

First QC Date

March 27, 2024

Last Update Submit

April 2, 2024

Conditions

Patients With Cicatricial EctropionOver 18-year-oldWith Complete Clinical Record

Outcome Measures

Primary Outcomes (1)

  • Ectropion Grading Scale

    The EGS describes the severity of the ectropion, with higher score for more severe ectropion.

    preoperative and one-year posttreatment

Study Arms (1)

Patients with ectropion underwent surgical treatment.

Other: Surgical treatment

Interventions

Surgical treatmentOTHER

Patients underwent surgical treatment of ectropion were included in this study.

Patients with ectropion underwent surgical treatment.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with ectropion underwent surgical treatment in our center.

You may qualify if:

  • patients with Cicatricial Ectropion;
  • over 18-year-old;
  • with complete clinical record.

You may not qualify if:

  • patients with severe complications

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shanghai ninth people's hospital

Shanghai, 200011, China

Location

MeSH Terms

Interventions

Surgical Procedures, Operative

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

March 27, 2024

First Posted

April 3, 2024

Study Start

December 12, 2023

Primary Completion

February 28, 2024

Study Completion

March 27, 2024

Last Updated

April 3, 2024

Record last verified: 2024-04

Locations

CN(1)