Sugar and sound waves: a new acne treatment?
NCT ID NCT07169890
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study tested whether applying a dextrose (sugar) gel with ultrasound, called phonophoresis, can improve mild to moderate acne. 115 people aged 18 to 30 with acne took part. The goal was to see if this approach reduces acne lesions and severity.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dextrose gel applied with ultrasound
- What this could lead to
- If it works, this could offer a non-drug treatment option for mild to moderate acne.
- What could go wrong
- This is a small, completed study with no phase designation, so results may not be conclusive or widely applicable. The treatment is experimental and not yet standard.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
115 people
The number who actually took part.
- Started
-
Nov 2025
- Finished
-
Dec 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 30 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Individuals aged 18 to 30 years. * Clinically diagnosed with mild to moderate acne vulgaris. * Willingness to comply with the study protocol and attend all treatment sessions. * Medical Clearance: Participants must have medical clearance to participate in this study. Exclusion Criteria: * Individuals with severe acne vulgaris or other dermatological conditions affecting the face. * Current use of systemic acne medications or topical treatments other than the study intervention. * Known allergy to magnesium or ultrasound gel. * Pregnant or breastfeeding individuals. * Severe Comorbidities: Individuals with severe cardiovascular, pulmonary, metabolic, or vascular diseases * Medication Interference: Individuals using medications known to affect presence of acne. * Acute Psychological Conditions: Participants with acute psychological conditions that may interfere with participation or assessments. * Obese patient whose BMI ≥ 30.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Acne vulgaris are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
faculty of physical therapy ,Cairo University
Cairo, 11311, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Acne may signal hidden hormonal disorder in young women
- Hormone tests may reveal who benefits most from acne drug
- Blood pressure drug takes on antibiotics for Women's acne
- Can radiofrequency waves outperform acne gels?
- Can adding a chemical peel to microneedling erase acne scars better?
- Can a beam of light boost acne treatment?