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Efficacy and Safety of STW 5-II for Functional Dyspepsia Treatment: A Patient Data-Based Meta-Analysis.
Andresen, Viola; Shah, Ayesha; Fink, Careen; Rabini, Sabine; Wargenau, Manfred; Holtmann, Gerald.
Afiliação
  • Andresen V; Medizinicum, Hamburg, Germany.
  • Shah A; Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Woolloongabba, Brisbane, Queensland, Australia.
  • Fink C; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Rabini S; Digestive Health and Phytomedicine, Steigerwald Arzneimittelwerk GmbH, Darmstadt, Germany.
  • Wargenau M; Digestive Health and Phytomedicine, Steigerwald Arzneimittelwerk GmbH, Darmstadt, Germany.
  • Holtmann G; M.A.R.C.O. GmbH and Co. KG, Institute for Clinical Research and Statistics, Düsseldorf, Germany.
Digestion ; 105(3): 166-174, 2024.
Article em En | MEDLINE | ID: mdl-38246134
ABSTRACT

INTRODUCTION:

Functional dyspepsia (FD) is a chronic relapsing gastroduodenal disorder with limited treatment options. Herbal products, like the six-herb combination STW 5-II, can target multiple FD gastrointestinal symptoms. In this meta-analysis, we evaluated the efficacy and safety of STW 5-II for overall FD, and key symptoms, based on Rome IV criteria.

METHODS:

We systematically screened the literature for randomized controlled clinical studies testing STW 5-II in FD. Meta-analysis was performed using data from individual patients with at least one key FD symptom (fullness, early satiety, or epigastric pain) of at least moderate severity at baseline. ANCOVA-based meta-analyses were performed on improvements in the total symptom sum score, and single symptoms, after 4 and 8 weeks. Safety data were analyzed by calculating odds ratios for all adverse events.

RESULTS:

Four randomized controlled trials, including 613 patients, were identified, and two were eligible for efficacy analysis. STW 5-II significantly improved the FD symptom sum score (mean difference of 1.74 after 4 weeks and 2.07 after 8 weeks) and key FD symptoms of fullness (0.28 and 0.29), early satiety (0.25 and 0.26), and epigastric/upper abdominal pain (0.26 and 0.3). Treatment-related or severe adverse events did not differ between STW 5-II and placebo.

CONCLUSION:

The results support that STW 5-II significantly improves FD symptoms after 4 and 8 weeks of treatment with no difference in relation to safety signals compared to placebo. Thus, STW 5-II can be considered an effective and safe treatment option for FD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Dispepsia Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Dispepsia Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article