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Recruiting Phase 4 NCT07544251

NCT07544251 Comparing Sarecycline and Doxycycline Effects on the Skin and Gut Bacteria in Acne.

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Clinical Trial Summary
NCT ID NCT07544251
Status Recruiting
Phase Phase 4
Sponsor Integrative Skin Science and Research
Condition Acne Vulgaris
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2026-04-20
Primary Completion 2027-04

Trial Parameters

Condition Acne Vulgaris
Sponsor Integrative Skin Science and Research
Study Type INTERVENTIONAL
Phase Phase 4
Enrollment 30
Sex ALL
Min Age 9 Years
Max Age N/A
Start Date 2026-04-20
Completion 2027-04
Interventions
SarecyclineDoxycycline

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Brief Summary

This study is being done to help better understand how the gut and skin bacteria of the body change when people with acne are treated with Sarecycline or Doxycycline. The bacteria in the gut and on the skin will be studied to see how each treatment may affect them and whether they change the profile of the bacteria that is present.

Eligibility Criteria

Inclusion Criteria: 1\) Diagnosis of acne vulgaris with: * At least 10 inflammatory lesions (papules, pustules, and nodules) up to 100 noninflammatory lesions (open and closed comedones) * No more than 2 nodules on the face Exclusion Criteria: 1. Dermatological condition of face or facial hair that could interfere with clinical evaluations 2. Subjects who have used the following medications (topical refers only to the facial area) will not be eligible: 2a) Within 2 week prior to randomization: * Topical acne medications such as retinoids, antibiotics, hormonal modulators * Topical benzoyl peroxide * Topical anti-inflammatories and corticosteroids 2b) Within 4 weeks prior to randomization: * Systemic antibiotics * Systemic acne treatments * Oral probiotic supplement * Systemic corticosteroids 2c) Within 12 weeks prior to randomization: * Systemic retinoids 3\) Individuals who have changed any of their hormonal based contraception or therapies within 3 months prior to joining the study.

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