Clinical Trials Directory

Trials / Terminated

TerminatedNCT00240513

Study Comparing Acne in Patients Taking Oral Minocycline to Patients Taking Minocycline Plus Topical Tretinoin

A Randomized Study to Compare the Acne Relapse Rate After a 3-mo Course of Oral Minocycline, to a 3-mo Course of Oral Minocycline in Combination With a Daily Dose of Topical Tretinoin 0.01% Followed by 3 mo of Topical Tretinoin Alone

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Derm Research @ 888 Inc. · Industry
Sex
All
Age
Healthy volunteers
Accepted

Summary

The use of oral antibiotics alone to treat inflammatory acne provides little to no long term therapeutic benefit. Acne relapse rates can be reduced by using topical tretinoin 0.01% in conjunction with minocycline, thereby increasing the therapeutic effect of the oral antibiotic.

Detailed description

Although oral antibiotics have been the mainstay of treatment of inflammatory acne for 30 years, studies comparing their efficacy have little scientific value. Evidence-based dermatology proves minocycline to be an effective treatment for acne vulgaris while the patient remains on the medication; however, the relapse rate of acne after a course of antibiotics has never been established. The relapse rate would appear to be significant, as repeated courses and long-term antibiotic use are commonly prescribed in practice. The increasing problem of drug resistance has raised issues of the suitability of such long term antibiotic treatment and this overuse is probably a contributing factor of multiple drug resistance in our society.

Conditions

Interventions

TypeNameDescription
DRUGMinocycline100 mg capsules OD for 3 months
DRUGMinocycline plus tretinoin100mg OD Minocycline for 12 weeks plus OD Topical tretinoin 0.01% for 12 weeks Followed by topical tretinoin 0.01% OD for 12 weeks alone

Timeline

Start date
2004-08-01
Primary completion
2006-12-01
Completion
2006-12-01
First posted
2005-10-18
Last updated
2012-02-24

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00240513. Inclusion in this directory is not an endorsement.