Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05582434 · ClinicalTrials.gov registry record · Early Phase 1

Experience With Topical Acne Treatment

A Early Phase 1 study of Acne, sponsored by Wake Forest University Health Sciences.

Active
Registry status
Early Phase 1
Development phase
72
Enrollment target
1
Study location

NCT05582434 is a Early Phase 1 study of Acne that is active but no longer recruiting, run by Wake Forest University Health Sciences. The registered enrollment target is 72 participants, below the 140-participant average among 26 other Acne trials with a reported enrollment target (49% lower). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05582434, a Early Phase 1 study of Acne, is active but no longer recruiting, sponsored by Wake Forest University Health Sciences.

ACTIVE NOT RECRUITING
Registry status
Early Phase 1
Development phase
72 participants
Enrollment target
1
Study location

Study Summary

Acne is a chronic condition that typically requires the use of multiple medications.1 Medication adherence is especially challenging for patients with chronic diseases and often decreases over time, especially for those using topical medications.1 Nonadherence can result in multiple negative effects including treatment failure, increased healthcare costs, and decreased quality of life. Primary nonadherence refers to problems acquiring and starting treatment. Challenges to this form of nonadherence include a lack of knowledge, misunderstanding of usage, poor communication with provider, increased cost, and fear of side effects.2 Secondary nonadherence refers to when the patient does not use the medication as prescribed. Hurdles to secondary nonadherence include delayed results, increased complexity of treatment plan, adverse effects, busy lifestyle, and inconvenience.2

Conditions Studied

Interventions

  • DRUG clindamycin phosphate 1.2%/adapalene 0.15%/BPO 3.1% gel
  • DRUG adapalene 0.3%/BPO 2.5% gel and compounded clindamycin phosphate 1.2% gel
  • DRUG Compounded BPO 2.5% gel, adapalene 0.1% gel, and compounded clindamycin phosphate 1.2% gel

Study Locations (1)

North Carolina

  • Wake Forest University Health Sciences - Winston-Salem

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2024-02-15
Est. Completion 2026-11
Phase Early Phase 1

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT05582434

The ClinicalTrials.gov registry entry for NCT05582434 describes a study currently listed as active not recruiting, categorized as Early Phase 1. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 140-participant average among 26 other Acne trials with a reported enrollment target (49% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Acne appearing as the primary indexed condition, and to 3 interventions - of which clindamycin phosphate 1.2%/adapalene 0.15%/BPO 3.1% gel is the first listed.

NCT05582434 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT05582434 about?

NCT05582434 is a clinical study titled "Experience With Topical Acne Treatment". Acne is a chronic condition that typically requires the use of multiple medications.1 Medication adherence is especially challenging for patients with chronic diseases and often decreases over time, especially for those using topical medications.1 Nonadherence can result in multiple negative effects...

What is the current status of trial NCT05582434?

This trial is currently active not recruiting. It is a Early Phase 1 study. The enrollment target is 72 participants. The study started on 2024-02-15. Estimated completion is 2026-11.

What conditions does trial NCT05582434 study?

This clinical trial studies the following conditions: Acne.

What interventions are being tested in trial NCT05582434?

The interventions under investigation include: clindamycin phosphate 1.2%/adapalene 0.15%/BPO 3.1% gel (DRUG), adapalene 0.3%/BPO 2.5% gel and compounded clindamycin phosphate 1.2% gel (DRUG), Compounded BPO 2.5% gel, adapalene 0.1% gel, and compounded clindamycin phosphate 1.2% gel (DRUG).

Who is sponsoring clinical trial NCT05582434?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05582434 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Acne

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.