Trial reportFrontiers in allergy2026
Homeopathic medication for seasonal allergic rhinitis-a randomised placebo-controlled trial.
Trial report in Frontiers in allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
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Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: The study aim was to evaluate the efficacy of homeopathic medication in SAR patients. Methods: In a double-blind, three-arm randomised trial, patients at eleven outpatient clinics and two medical centres were randomised to receive (1) individualised homeopathic case taking (IHCT) and standardised homeopathic medication with Galphimia Glauca (GG), (2) IHCT and individualised homeopathic treatment (IHG), or (3) IHCT and placebo (PG). Primary outcome was disease-specific quality of life, assessed using the Rhinitis Quality of Life Questionnaire (RQLQ) after three and four weeks. Secondary outcomes included response rate (≥0.5-point change in RQLQ), rescue medication use, and total nasal and non-nasal symptom scores (TNSS, TNNSS). Results: Sixty-two SAR patients (mean age ± SD: 46.9 ± 14.9; 43.5% female) were recruited, approximately 25% of the planned sample size. After weeks three and four, there were no significant differences in RQLQ ( Conclusion: Standardised and individualised homeopathic drugs were not superior compared to placebo suggesting that treatment response was not based on study medication. The validity of the study and its conclusions are limited by the fact that the recruitment target was not achieved. Trial registration: This study has been registered in the German Clinical Trial Registry with trial ID DRKS00018081.
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