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NCT01333150

Effects of a Low-dose Propranolol on a Stress Induced Autonomic Response and on Muscle Pain

Status unknown NA Last updated 23 March 2012
What this trial tests

NA trial testing Propranololhydrochlorid in Temporomandibular Joint Disorders in 16 participants. Status unknown.

Timeline
1 August 2011
Primary endpoint
1 September 2012
1 September 2012

Quick facts

Lead sponsorUniversity of Aarhus
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposebasic science
Enrollment16
Start date1 August 2011
Primary completion1 September 2012
Estimated completion1 September 2012
Sites2 locations across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

University of Aarhus

Who can join

Adults 18 to 60, female only, with Temporomandibular Joint Disorders or Myofascial Temporomandibular Disorders. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The project's primary purpose is to test the hypothesis that oral administration of a low single dose of β-antagonist propranolol (40 mg) reduces pain sensitivity in patients with masticatory muscle pain.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Temporomandibular Joint Disorders

Currently open trials in the same condition.

Other University of Aarhus 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/NCT01333150.

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