# Efficacy of topical erythropoietin gel and mouthwash for recurrent aphthous stomatitis in a randomized clinical trial

**Authors:** Mai Talaat Elgendi, Radwa R. Hussein, Nivine Ragy, Nada M. El Hoffy, Nevine H. Kheir El Din

PMC · DOI: 10.1038/s41598-026-40440-7 · 2026-03-18

## TL;DR

A clinical trial found that erythropoietin gel is effective in reducing pain and healing mouth ulcers in patients with Recurrent Aphthous Stomatitis.

## Contribution

This study is the first to demonstrate that EPO gel is more effective than mouthwash and placebo in treating RAS.

## Key findings

- EPO gel significantly reduced pain, ulcer size, and salivary IL-2 levels compared to placebo.
- Patients using EPO gel had longer recurrence-free intervals (median 5 months) compared to other groups.
- EPO gel showed nearly total pain relief and significant ulcer healing.

## Abstract

Erythropoietin (EPO) has anti-inflammatory, antioxidant, and wound-healing properties that could be valuable in managing Recurrent Aphthous Stomatitis (RAS). This study aimed to evaluate its clinical effectiveness in either gel in orabase or mouthwash, on pain reduction, ulcer healing, recurrence rates, and salivary IL-2 level in patients with RAS. In this randomized clinical trial, 60 patients with RAS were equally divided into 3 groups: EPO oral gel, EPO mouthwash, or a placebo. Ulcer size, the Pain Visual Analog Scale (P-VAS), and salivary IL-2 levels were evaluated at baseline, day 3, and day 7. When compared to a placebo, both EPO formulations significantly decreased pain, ulcer size, and salivary IL-2 levels (p < 0.001). With nearly total pain relief, significant ulcer healing, and the lowest post-treatment IL-2 concentration, the EPO gel group showed the greatest improvement. In comparison to mouthwash and a placebo, patients treated with EPO gel also had noticeably longer recurrence-free intervals (median 5 months). No negative effects noted. These findings suggest that EPO gel is a therapeutic option for RAS that is both safe and effective, with the potential to modify the disease in addition to relieving symptoms.

Trial registration: The study was registered at Clinical Trials.gov (NCT06923605) on 11/4/2025.

## Linked entities

- **Proteins:** IL2 (interleukin 2)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Il2 (interleukin 2) [NCBI Gene 116562], IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, Il18 (interleukin 18) [NCBI Gene 29197] {aka IL-1 gamma, IL-18}, Epo (erythropoietin) [NCBI Gene 24335], IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}
- **Diseases:** weight gain (MESH:D015430), Ulcer (MESH:D014456), nausea (MESH:D009325), impairment (MESH:D060825), infections (MESH:D007239), oral disorders (MESH:D009056), erythema (MESH:D004890), mucosal lesions (MESH:D009059), itching (MESH:D011537), tongue defects (MESH:D014060), depression (MESH:D003866), cancer (MESH:D009369), adrenal suppression (MESH:D000310), mucosal atrophy (MESH:D001284), chronic (MESH:D002908), immunoinflammatory dysfunction (MESH:D006331), mucosal irritation (MESH:D001523), oral candidiasis (MESH:D002180), mucositis (MESH:D052016), Pain (MESH:D010146), intellectual disabilities (MESH:D008607), psychosomatic disorders (MESH:D011602), Aphthous Stomatitis (MESH:D013281), system (MESH:D015619), allergic reactions (MESH:D004342), RAS (MESH:C538145), inflammation (MESH:D007249), systemic diseases (MESH:D034721), anxiety (MESH:D001007), headache (MESH:D006261), oral mucositis (MESH:D013280)
- **Chemicals:** RAU (-), colchicine (MESH:D003078), triethanolamine (MESH:C009546), triamcinolone acetonide (MESH:D014222), pentoxifylline (MESH:D010431), oxygen (MESH:D010100), steroid (MESH:D013256), Carbopol (MESH:C006912), polypropylene (MESH:D011126), lipid (MESH:D008055), NaCl (MESH:D012965), TMB (MESH:C021758), water (MESH:D014867), HA (MESH:D006820), orabase (MESH:C056627), prednisone (MESH:D011241)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13002904/full.md

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Source: https://tomesphere.com/paper/PMC13002904