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Evaluation of the antipruritic effects of topical pimecrolimus in non-atopic prurigo nodularis: results of a randomized, hydrocortisone-controlled, double-blind phase II trial.

AbstractBACKGROUND:
In the treatment of atopic dermatitis, pimecrolimus has high antipruritic effects.
OBJECTIVE:
To investigate the efficacy of 1% pimecrolimus cream in comparison to 1% hydrocortisone cream in non-atopic prurigo nodularis (PN).
METHODS:
A randomized, controlled, double-blind study with intraindividual randomization was done in 30 patients (17 females, 13 males; mean age 58.5 years) with PN.
RESULTS:
Pruritus intensity decreased significantly (p < 0.001) on both treated sides as early as after 10 days of treatment; scratch lesions improved (p < 0.001). Quality of life as assessed by the Dermatology Life Quality Index improved significantly. However, a significant advantage of pimecrolimus over hydrocortisone was not found.
CONCLUSION:
The results suggest that the non-steroid pimecrolimus is an effective alternative for PN treatment.
AuthorsDorothee Siepmann, Tobias Lotts, Christine Blome, Matthias Braeutigam, Ngoc Quan Phan, Trude Butterfass-Bahloul, Matthias Augustin, Thomas A Luger, Sonja Ständer
JournalDermatology (Basel, Switzerland) (Dermatology) Vol. 227 Issue 4 Pg. 353-60 ( 2013) ISSN: 1421-9832 [Electronic] Switzerland
PMID24281309 (Publication Type: Clinical Trial, Phase II, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Inflammatory Agents
  • Biomarkers
  • Dermatologic Agents
  • Neuropeptides
  • pimecrolimus
  • Calcitonin Gene-Related Peptide
  • Hydrocortisone
  • Tacrolimus
Topics
  • Administration, Cutaneous
  • Adult
  • Aged
  • Anti-Inflammatory Agents (therapeutic use)
  • Biomarkers (metabolism)
  • Calcitonin Gene-Related Peptide (metabolism)
  • Dermatologic Agents (administration & dosage)
  • Double-Blind Method
  • Female
  • Humans
  • Hydrocortisone (therapeutic use)
  • Male
  • Middle Aged
  • Neuropeptides (metabolism)
  • Prurigo (complications, drug therapy, metabolism)
  • Pruritus (drug therapy, etiology, metabolism)
  • Quality of Life
  • Tacrolimus (administration & dosage, analogs & derivatives)

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