Your browser doesn't support javascript.
loading
Efficacy and safety of purslane (Portulaca oleracea) for mild to moderate chronic hand eczema; A randomized, double-blind, placebo-controlled clinical trial.
Heydarirad, Ghazaleh; Rastegar, Sedigheh; Haji-Abdolvahab, Habibbolah; Fuzimoto, Andréa; Hunter, Jennifer; Zare, Roghayeh; Pasalar, Mehdi.
Affiliation
  • Heydarirad G; Traditional Medicine and Materia Medica Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Department of Traditional Medicine, School of Traditional Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Rastegar S; Department of Traditional Medicine, School of Traditional Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Haji-Abdolvahab H; Department of Statistics and Information Technology, University of Tehran, Tehran, Iran.
  • Fuzimoto A; Holistic Sync, Holistic Integrative Medicine, USA.
  • Hunter J; Director, Health Research Group, Sydney, New South Wales, Australia.
  • Zare R; Research Center of Persian Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
  • Pasalar M; Research Center for Traditional Medicine and History of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: pasalar@sums.ac.ir.
Explore (NY) ; 2023 Oct 11.
Article in En | MEDLINE | ID: mdl-37872023
ABSTRACT

INTRODUCTION:

Chronic hand eczema (CHE) is a common skin inflammation with a complex pathophysiology. Due to its anti-inflammatory properties, Portulaca oleracea L. (purslane) is traditionally used in Persian medicine for skin ailments. This study aimed to evaluate the safety and efficacy of a standardized purslane extract (based on traditional Persian medicine) for adults with mild or moderately severe CHE.

METHODS:

A randomized, double-blind, placebo-controlled clinical trial was conducted at Razi Hospital in Iran from January to June 2022. Participants were randomly allocated to receive an oral purslane or placebo syrup plus topical Vaseline for four weeks. Seventy participants were randomly allocated into the intervention (n = 35) and placebo (n = 35) groups. The primary outcomes were the extent and severity of CHE symptoms over the four weeks after adjusting for age, gender and baseline score. Secondary outcomes were quality of life, symptom recurrence, treatment satisfaction, and adverse events.

RESULTS:

After 4 weeks of treatment, compared to the placebo group (n = 31), the purslane group (n = 31) had significantly lower physician-reported fissure scores (adjusted mean difference (adjMD) -0.50, 95 %CI -3.93 to -0.34, p = 0.043), participant-reported itching (adjMD -0.51, 95 %CI -2.32 to -0.31, p = 0.041), dryness (adjMD -1.46, 95 %CI -2.89 to -0.03, p = 0.045), and total itching, dryness and thickness (adjMD -2.36, 95 %CI -6.23 to -1.51, p = 0.023) scores. Fourteen participants (purslane n = 10; placebo n = 4, p = 0.068) experienced adverse events of mild to moderate severity.

CONCLUSION:

Purslane has some promising effects for reducing the extent and severity of CHE symptoms, and no direct comparisons have been made with commonly used treatments. Future multicenter trials and mechanistic studies are warranted to establish the safety and effectiveness of purslane as a potential therapeutic agent for CHE. TRIAL REGISTRATION Iranian Registry of Clinical Trials (IRCT20200707048040N1).
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Explore (NY) Journal subject: TERAPIAS COMPLEMENTARES Year: 2023 Document type: Article Affiliation country: Irán

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Explore (NY) Journal subject: TERAPIAS COMPLEMENTARES Year: 2023 Document type: Article Affiliation country: Irán