New combo treatment for vitiligo shows promise in early trial
NCT ID NCT07563049
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether injecting carbon dioxide gas (carboxytherapy) alongside standard narrowband UVB light therapy can improve repigmentation in people with stable vitiligo. Fifty-nine participants with symmetrical patches will receive whole-body UVB light, with carboxytherapy added on one side only. The study measures changes in skin color and certain blood markers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- carbon dioxide gas
- What this could lead to
- If it works, this could offer a better way to restore skin color in people with stable vitiligo.
- What could go wrong
- This is a small, early-phase trial with only 59 people. The added benefit of carboxytherapy may be small or none, and injections can cause discomfort or bruising.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
59 people
The number who actually took part.
- Started
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Sep 2024
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- 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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Subjects with stable non-segmental vitiligo (≥2 symmetrical patches of diameter less than 2 cm on acral or ≥ 2 symmetrical patches on non-acral sites). Subjects were stable for twelve or more months. Exclusion Criteria: * Subjects with unstable vitiligo. * Subjects with segmental vitiligo. * Pregnant females. * Severe anemia (Hb \<7 gm/dl). * Cardiac/hepatic/renal/respiratory failure. * Superficial thrombophlebitis. * Subjects with history of skin malignancy or precancerous conditions like Xeroderma pigmentosum. * Subjects with other autoimmune disorders. * Systemic drugs for vitiligo in the last 3 months.
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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 Medicine, Cairo University
Cairo, El Manial, 11956, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.