About this trial
Acne vulgaris is a persistent inflammatory condition of the pilosebaceous unit, affecting 85% of people between the ages of 12 and 24, it is regarded as one of the most common diseases in teenagers and young adults.
Catestatin, a peptide derived from chromogranin A (CgA), was first discovered in 1997 as an acute nicotinic-cholinergic antagonist. Later, it was determined that CST is a pleiotropic hormone.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Healthy persons of both sexes with moderate and severe acne.
Disqualifiers
Pregnant and lactating women.
Immunocompromised patients.
Severe anemia.
History of chronic liver disease.
Trial design
Parallel
Treatments tested in this trial
Isotretinoin
Drug* Measure the serum levels of catestatin in patients with moderate and severe acne vulgaris versus healthy control persons. * Evaluate the effect of oral isotretinoin treatment on serum catestatin levels in patients with moderate and severe acne vulgaris.
Treatment groups
Trial outcomes
Primary outcomes
Evalaute serum level of Catestatin in acne patient
Assessment of clinical improvement according to:(8) G4(excellent:100% reduction) G3(good:75-99% reduction) G2(moderate: 50-74% reduction) G1(insufficient :1-49% reduction) G0(unchanged) G-1(worse)
Evalaute the effect of treatment with systemic isotretinon
Evaluate the effect of treatment with systemic isotretinon therapy (0.5 mg/kg/day, up to 40 mg daily) on the level of serum Catestatin on the Participants whom suffering from Acne Vulgaris whether moderate or severe.
Sponsors and contacts
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