Evidence map›Paper›PMID 42321377›Full record

Trial reportScientific reports2026

An oral nutritional supplement with TRPM8 agonists as a cooling flavor improved swallowing function in post-stroke patients with oropharyngeal dysphagia.

Noemí Tomsen, Daniel Españó, Adrian Nuñez-Lara, Pere Clavé

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Noemí TomsenCentro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Madrid, Spain. ntomsen@csdm.cat.ORCID https://orcid.org/0000-0001-7149-7948
Daniel EspañóGastrointestinal Physiology Lab, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Mataró, Spain.ORCID http://orcid.org/0000-0002-3378-1160
Adrian Nuñez-LaraCentro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Madrid, Spain.ORCID http://orcid.org/0009-0004-3000-5619
Pere ClavéCentro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Madrid, Spain.ORCID http://orcid.org/0000-0002-0696-8560

Funding

Instituto de Salud Carlos III ICI25/00044Instituto de Salud Carlos III PI22/01101
6 · The paper itself

Abstract

Post-stroke patients with OD (PSOD) show impaired oropharyngeal sensory function, impaired safety during voluntary swallow (VS) and a critical reduction of spontaneous swallowing frequency (SSF), increasing the risk of aspiration of oropharyngeal secretions. Our aim was to evaluate the effect of oropharyngeal sensory stimulation on the VS and SSF in chronic PSOD patients using a cooling sensation flavoring (TRPM8 agonists) in an oral nutritional supplement (ONS) drink and comparing it with a control ONS. We performed a prospective, crossover, interventional and open-label clinical study on 50 PSOD patients. Patients were randomized into two groups, which differed from each other according to the order in which the ONS were administered: (1) Group A (n = 25): 1st visit, cooling sensation (active) + 2nd visit, control; and (2) Group B (n = 25): 1st visit, control + 2nd visit, active. The swallowing function was evaluated pre and post administration of each product using the volume-viscosity swallowing test (V-VST) for the VS, including the prevalence of impaired safety and efficacy, and SSF (swallows/minute). A saliva sample before and after the administration of control and active ONS' was collected to quantify substance P (SP) and calcitonin gen-related peptide (CGRP) by using ELISA. We observed that mean basal SSF in PSOD was low (0.29 ± 0.21 swallows/min). PSOD patients showed a significant increase in SSF (51.6%, p < 0.0001), a 22% (p = 0.0449) reduction in the prevalence of impaired safety during VS and a 15% (p = 0.0453) increase in the concentration of salivary SP after the administration of the active ONS. In contrast, no significant changes were observed after the administration of the control product. The order of administration did not affect the results. In conclusion, the TRPM8 compound included in the active ONS facilitates sensory perception, enhancing the peripheral release of SP and improving SSF and safety of swallow during VS in PSOD, which suggests both cortical, and brainstem enhancement of swallow responses.

Indexed as

DeglutitionDeglutition DisordersDietary SupplementsStrokeTRPM Cation ChannelsAdministration, OralAgedCross-Over StudiesFemaleHumansMaleMiddle AgedProspective StudiesTRPM8 protein, humanTRPM Cation ChannelsInvoluntary swallowingNeurostimulationStrokeSwallowing disordersTransient receptor potential channelsVoluntary swallowing

Identifiers

PMID42321377
PMCPMC13572451

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.