Trial record 2 of 156 for:
Open Studies | "Psoriasis"
Non-interventional Study of Long-term Treatment of Psoriasis With Calcipotriol Plus Betamethasone in Gel Formulation
This study is currently recruiting participants.
Verified October 2012 by LEO Pharma
Sponsor:
LEO Pharma
Information provided by (Responsible Party):
LEO Pharma
ClinicalTrials.gov Identifier:
NCT01707368
First received: October 12, 2012
Last updated: NA
Last verified: October 2012
History: No changes posted
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Purpose
The purpose of this observational study is to document the course of disease and relapse management during treatment with Daivobet® Gel under consideration of patient`s individual application habits under daily use conditions.
| Condition | Intervention |
|---|---|
|
Psoriasis Vulgaris Plaque Psoriasis |
Drug: Daivobet® Gel |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Course of Psoriasis During Long Term Treatment With Calcipotriol Plus Betamethasone in Gel Formulation |
Resource links provided by NLM:
MedlinePlus related topics:
Psoriasis
Drug Information available for:
Betamethasone sodium phosphate
Betamethasone
Betamethasone valerate
Betamethasone dipropionate
Calcipotriene
Daivobet
U.S. FDA Resources
Further study details as provided by LEO Pharma:
Primary Outcome Measures:
- The course of disease and relapse management during treatment with Daivobet® Gel under consideration of patient`s individual application habits under daily use conditions. [ Time Frame: 1 year ] [ Designated as safety issue: No ]Number of exacerbations and relapses during one year observation time
Secondary Outcome Measures:
- Physician's global Assessment of psoriasis vulgaris [ Time Frame: 1 year ] [ Designated as safety issue: No ]Assessment on 6-step scale from "no visible disease (O)" to "very severe disease (5)
- Side effects [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]Number of participants with serious and non-serious adverse drug reactions, according to organ classes.
| Estimated Enrollment: | 1000 |
| Study Start Date: | October 2012 |
| Estimated Study Completion Date: | June 2014 |
| Estimated Primary Completion Date: | March 2014 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
all eligible patients
Daivobet® Gel once daily on areas with plaque psoriasis, treatment duration up to 8 weeks for body skin areas except scalp (scalp up to 4 weeks), treatment may be repeated under medical surveillance.
|
Drug: Daivobet® Gel
Once daily on areas with plaque psoriasis, treatment duration up to 8 weeks for body skin areas except scalp (scalp up to 4 weeks), treatment may be repeated under medical surveillance.
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
Patients with Psoriasis vulgaris visiting their attending dermatologist in the primary care clinic
Criteria
Inclusion Criteria:
- Patients with light to moderate psoriasis vulgaris of trunk and extremities and treatment with Daivobet® Gel was planned anyway.
- Minimum of 3 years diagnosed psoriasis vulgaris.
Exclusion Criteria:
- Previous therapy with Daivobet® Gel
- Systemic therapy of psoriasis vulgaris
- Contraindications of Daivobet® Gel in the German package insert
- people that are incapable to give free consent
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01707368
Contacts
| Contact: Tobias Anger | +49 6102 201 258 | tobias.anger@leo-pharma.com |
Locations
| Germany | |
| PD Dr. med. Rosenbach | Recruiting |
| Osnabrück, Niedersachsen, Germany, 49078 | |
| Contact: Thomas Rosenbach, PD Dr.med. +49541335000 info@IhreHautaerzte.de | |
Sponsors and Collaborators
LEO Pharma
Investigators
| Principal Investigator: | Thomas Rosenberg, PD Dr. med. | private practise, D- 49078 Osnabrück, Germany |
More Information
No publications provided
| Responsible Party: | LEO Pharma |
| ClinicalTrials.gov Identifier: | NCT01707368 History of Changes |
| Other Study ID Numbers: | DE-Daivobet-longterm-NIS-2012 |
| Study First Received: | October 12, 2012 |
| Last Updated: | October 12, 2012 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
Keywords provided by LEO Pharma:
|
Psoriasis Psoriasis vulgaris Plaque Psoriasis Daivobet® Gel Germany |
Additional relevant MeSH terms:
|
Psoriasis Skin Diseases, Papulosquamous Skin Diseases Betamethasone-17,21-dipropionate Betamethasone Betamethasone sodium phosphate Calcipotriene Anti-Inflammatory Agents Therapeutic Uses |
Pharmacologic Actions Anti-Asthmatic Agents Respiratory System Agents Glucocorticoids Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Dermatologic Agents |
ClinicalTrials.gov processed this record on May 22, 2013