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Effect of GLP-1 Analogs on Psoriasis in Type 2 Diabetic Patients

Clinical and Histopathological Effect of GLP-1 Analogs on Psoriasis in Type 2 Diabetic Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01687582
Enrollment
10
Registered
2012-09-19
Start date
2012-01-31
Completion date
2013-03-31
Last updated
2019-03-12

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

Conditions

Type 2 Diabetes, Psoriasis

Keywords

type 2 diabetes, psoriasis, exenatide, liraglutide

Brief summary

The aim of the study is to evaluate after 4 to 6 months the effects of a GLP-1 analog treatment on psoriatic skin lesions in patients with type 2 diabetes.

Detailed description

The objective of this study is to analyse short and medium-term efficacy on clinical, immunological and histopathological parameters of a GLP-1 receptor agonist on moderate to severe psoriasis plaques in a group of patients with type 2 diabetes.

Interventions

GLP-1 analog treatment

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Type 2 diabetic patients treated with oral anti-hyperglycaemic agents and/or insulin and presenting stable psoriasis plaques for at least one year, which failed to respond to previous systemic and/or topical treatments.

Exclusion criteria

* Type 1 diabetes * Secondary diabetes * Liver, renal or pancreatic disease * Previous treatment with GLP-1 agonist or DPP-4 inhibitors agents

Design outcomes

Primary

MeasureTime frame
Improvement of PASI score4 to 6 months

Secondary

MeasureTime frameDescription
Evolution of immunological data4 to 6 monthscytokines and T cells
Evolution of histopathological data4 to 6 monthsthickness, dermis infiltrate in skin plaques and in control areas
Evolution of BMI (body mass index)4 to 6 monthsnumber of patients with weight loss
Evolution of routine laboratory measures4 to 6 monthsnumber of participants with biological adverse effects (pancreatitis enzymes)
Evolution of BMI4 to 6 monthsweight
Evolution of glycaemic control4 to 6 monthsHbA1c

Countries

Belgium

Outcome results

None listed

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