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Lifestyle Modification in Psoriatic Patients With Fatty Liver

Response of Fatty Liver to Lifestyle Modification in Psoriasis Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05125757
Enrollment
60
Registered
2021-11-18
Start date
2021-09-13
Completion date
2022-03-15
Last updated
2021-11-18

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

Conditions

Fatty Liver, Psoriasis

Brief summary

Several recent reports have shown an increased prevalence of nonalcoholic fatty liver disease (NAFLD) in those with psoriasis, which may reflect the increased occurrence of metabolic syndrome in this patient population.

Detailed description

the recruitment of 60 fatty live men with chronic disease, psoriasis, will be classified to lifestyle modification group (foe 12 weeks, this patients will take supervised energy or diet restriction program plus their usual immunosuppressive drugs ) and control group will continue their drug program only)

Interventions

OTHERlifestyle modification

for 12 week, the patients of this group will receive their usual immuno-modulating therapy plus life style modification (energy or diet restriction in addition to daily walking, 15000 steps)

OTHERusual lifestyle

the patients will receive the usual immuno-modulating therapy with continued usual diet and activities

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* psoriasis obese patients with coexisting fatty liver * chronic plaque psoriasis * patients who will not show any change in immuno-modulating psoriasis therapies for at least five months before participation in the study.

Exclusion criteria

* no metabolic syndrome * no renal or cardiac or pulmonary disorders * other types of psoriasis

Design outcomes

Primary

MeasureTime frameDescription
Psoriasis Area and Severity IndexIt will be measured after 12 weeksit is an index used to measure level and severity of psoriasis

Secondary

MeasureTime frameDescription
triglyceridesIt will be measured after 12 weekswill measured in plasma
ASTIt will be measured after 12 weeksit is plasma aspartate transaminase
Dermatology Life Quality IndexIt will be measured after 12 weeksit is a questinnaire used to assess life quality in psoriasis humans
BMIIt will be measured after 12 weeksit is body mass index
waist circumferenceIt will be measured after 12 weeksit will be measured at the level of umbilicus
ALTIt will be measured after 12 weeksit is plasma Alanine transaminase

Countries

Egypt

Contacts

Primary ContactAli Ismail, lecturer
allooka2012@gmail.com02 01005154209

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026