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Myorelaxant Effect of Cannabis Cream Topical Skin Application in Patients With TMD

Myorelaxant Effect of Cannabis Cream Topical Skin Application in Patients With Temporomandibular Disorders: a Randomized, Double-blind Study

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03994640
Enrollment
20
Registered
2019-06-21
Start date
2018-01-01
Completion date
2019-01-01
Last updated
2019-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis, Electromyography, Myofascial Pain, Temporomandibular Disorder

Keywords

temporomandibular disorder, Cannabis, Electromyography, Masticatory muscles, Topical application

Brief summary

Evaluation of myorelaxant effect of cannabis cream.compared to placebo cream in topical skin application in patients with TMD

Detailed description

Cannabis sativa has a very wide application in various fields of medicine. In patients with temporomandibular disorder, especially with myofascial pain of masticatory muscles there is a special need to seek an effective pain therapy and muscle relaxing methods. Patients with TMD suffer from chronic pain and depression, cannabis topical skin application therapy seems promising in that field. Patients attending The Department of TMD in Zabrze, Polska were randomly divided into two groups: experimental and placebo. sEMG activity values were compared during 14 days therapy with cream. Positive results were obtained confirming the efficacy of the cannabis cream used in the study, compared to placebo.

Interventions

COMBINATION_PRODUCTCannabis Cream

Topical, bilateral skin application of cannabis cream with self-massage of masseter muscles

COMBINATION_PRODUCTPlacebo Cream

Topical, bilteral skin application of placebo cream with self-massage of masseter muscles

Sponsors

Medical University of Silesia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Masking description

double blind study: for patients and researchers

Intervention model description

two groups parallel study: experimental and control group

Eligibility

Sex/Gender
ALL
Age
22 Years to 27 Years
Healthy volunteers
Yes

Inclusion criteria

The inclusion criteria were as follows: 1. Patient agreement to participate into the research study 2. Age ≥22 and ≤ 27 3. Good general health, 4. Temporomandibular disorder-positive RDC/TMD examination for group Ia and Ib 5. Presence of all teeth (with the exception of the third molars) The

Exclusion criteria

were: 1. Cannabis cream/ placebo cream allergy 2. Hypersensitivity to substances to be used in the study 3. Skin wounds with skin surface discontinuation 4. Addiction to cannabis 5. Patients being treated with analgesic drugs and/or drugs that affect muscle function 6. Fixed or removable dental prosthesis 7. Disease or autoimmune disorder associated with generalized muscular tension

Design outcomes

Primary

MeasureTime frameDescription
Reduction of sEMG activity of masseter muscle14 daysReduction in masseter muscle electromyographic activity

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026