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NCT05729529

Impact of Alpha Lipoic Acid Efficacy in Burning Mouth Syndrome

Status unknown NA Last updated 15 February 2023
What this trial tests

NA trial testing Lipoid acid gel in Burning Mouth Syndrome in 60 participants. Status unknown.

Timeline
20 January 2020
Primary endpoint
25 May 2023
30 May 2023

Quick facts

Lead sponsorUniversity of Catania
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment60
Start date20 January 2020
Primary completion25 May 2023
Estimated completion30 May 2023
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

University of Catania

Who can join

Adults 18 to 75, any sex, with Burning Mouth Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A double-blind placebo-controlled trial is conducted in order to evaluate the efficacy of alpha lipoic acid (ALA) and determine the statistical significance of the outcome variables. Burning mouth syndrome (BMS) is defined as an oral burning sensation in the absence of clinical signs which could justify the syndrome. Recent studies suggest the existence of neurological factors as a possible cause of the disease.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Burning Mouth Syndrome

Currently open trials in the same condition.

Other University of Catania trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05729529.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing