Study of the Safety and Efficacy of Moxidectin Tablets for the Reduction of Demodex Eyelash Infestation

NCT ID: NCT06795165

Last Updated: 2025-08-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-02

Study Completion Date

2025-06-15

Brief Summary

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A Single-Center, Investigator-Masked, Randomized, Placebo-Controlled, Investigator Initiated Study of the Safety and Efficacy of Moxidectin Tablets for the Reduction of Demodex Eyelash Infestation

Detailed Description

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Conditions

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Blepharitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Active

Group Type ACTIVE_COMPARATOR

Moxidectin 2 MG Oral Tablet

Intervention Type DRUG

active medication

Active and Placebo

Group Type EXPERIMENTAL

Moxidectin 2 MG Oral Tablet

Intervention Type DRUG

active medication

Placebo

Intervention Type DRUG

placebo pills

Placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

placebo pills

Interventions

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Moxidectin 2 MG Oral Tablet

active medication

Intervention Type DRUG

Placebo

placebo pills

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

\- Active blepharitis with collarettes

Exclusion Criteria

* Other clinically significant eye disease
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eye Research Foundation, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Eye Research Foundation, Inc.

Newport Beach, California, United States

Site Status

Countries

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United States

Other Identifiers

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MOX-001

Identifier Type: -

Identifier Source: org_study_id

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