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Efficacy and Safety of Acitretin Plus Pioglitazone in Patients With Psoriasis
This study is not yet open for participant recruitment.
Verified by Postgraduate Institute of Medical Education and Research, November 2006
First Received: November 3, 2006   No Changes Posted
Sponsored by: Postgraduate Institute of Medical Education and Research
Information provided by: Postgraduate Institute of Medical Education and Research
ClinicalTrials.gov Identifier: NCT00395941
  Purpose

Acitretin, when given in combiantion with pioglitazone might achieve better and/or more rapid control of moderate to severe chronic plaque type psoriasis.


Condition Intervention Phase
Psoriasis
Drug: Pioglitazone
Phase II

MedlinePlus related topics: Psoriasis
Drug Information available for: Pioglitazone Pioglitazone hydrochloride
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Further study details as provided by Postgraduate Institute of Medical Education and Research:

Primary Outcome Measures:
  • Change in PASI score from baseline in the two groups

Secondary Outcome Measures:
  • Proportion of subjects with an improvement of at least 75% in the psoriasis area-and-severity index (PASI) by week 12

Estimated Enrollment: 40
Study Start Date: December 2006
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Patients with chronic plaque type psoriasis having body surface area involvement of > 20%
  • Patients of either sex
  • Females who have completed their family and are tubectomized or are postmenopausal i.e. no menstrual bleeding over at least 1 year
  • Age range 18-65 years

Exclusion Criteria:

  • Females of child bearing potential
  • H/O hypersensitivity to acitretin
  • Impaired hepatic function (serum bilirubin, AST, ALT and alkaline phosphatase >1.5 times the upper limit of normal)
  • Impaired renal function (serum creatinine >1.5mg% in males and >1.4 mg% in females)
  • Hyperlipidemia
  • BMI >30 kg /m2
  • H/O excessive alcohol use
  • Diabetes mellitus
  • Congestive heart failure
  • Ischemic heart disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00395941

Contacts
Contact: Samir Malhotra, MD, DM +91-172-2755243 samirmalhotra345@yahoo.com

Locations
India
PGIMER
Chandigarh, India, 160012
Sponsors and Collaborators
Postgraduate Institute of Medical Education and Research
Investigators
Study Chair: Sunil Dogra, MD PGIMER
  More Information

No publications provided by Postgraduate Institute of Medical Education and Research

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Study ID Numbers: Pharma 6/699
Study First Received: November 3, 2006
Last Updated: November 3, 2006
ClinicalTrials.gov Identifier: NCT00395941     History of Changes
Health Authority: India : PGIMER

Study placed in the following topic categories:
Hypoglycemic Agents
Pioglitazone
Skin Diseases
Psoriasis
Acitretin
Skin Diseases, Papulosquamous

Additional relevant MeSH terms:
Hypoglycemic Agents
Pioglitazone
Skin Diseases
Psoriasis
Physiological Effects of Drugs
Skin Diseases, Papulosquamous
Pharmacologic Actions

ClinicalTrials.gov processed this record on May 07, 2009