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Comparative Efficacy of Alpha Hydroxy Acids With and Without Nanocarriers Versus Calcipotriol Plus Betamethasone in Treatment of Plaque Psoriasis

Comparative Efficacy of Alpha Hydroxy Acids With and Without Nanocarriers Versus Calcipotriol Plus Betamethasone in Treatment of Plaque Psoriasis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07816575
Enrollment
80
Registered
2026-09-11
Start date
2024-03-15
Completion date
2025-09-10
Last updated
2026-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis

Brief summary

The aim of this double blind comparative clinical study is to evaluate the efficacy of AHAs combined with nanocarriers and their use as a non steroidal alternative drug for long term management of plaque psoriasis

Interventions

DRUGAlpha Hydroxy Acids with nanocarriers

Topical Alpha Hydroxy Acids formulated with nanocarriers applied to psoriatic plaques.

DRUGAlpha Hydroxy Acids only.

Topical Alpha Hydroxy Acids only applied to psoriatic plaques.

Topical calcipotriol plus betamethasone ointment applied to psoriatic plaques.

Vehicle control / Placebo topical application applied to psoriatic plaques

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

- Mid to moderate cases according to Psoriasis Area and Severity Index (PASI). * Age from18-65 years old. * Denovo psoriatic patients and patients with no psoriasis therapy in the previous two months.

Exclusion criteria

* Severe irritation and highly inflamed skin. * Pregnant and lactating females. * Patients with acute renal insufficiency. * Face, flexural and groin lesions.

Design outcomes

Primary

MeasureTime frameDescription
Percentage Change in PASI Score.Baseline and 8 weeksReduction in PASI score from baseline to week 8.

Secondary

MeasureTime frameDescription
Dermatology Life Quality Index (DLQI)Baseline and 8 weeks).Changes in DLQI score to assess the impact of treatment on patients' quality of life.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 12, 2026