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Effects of Dry Needling in Patients With Sleep Bruxism and Temporomandibular Disorders: a Prospective Case Series

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02587182
Enrollment
17
Registered
2015-10-27
Start date
2015-06-30
Completion date
2015-11-30
Last updated
2016-06-03

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

Conditions

Myofascial Pain

Brief summary

The objective of the present study was to assess the effectiveness of deep dry needling in the masseter and temporalis MTrPs on pain, pressure pain threshold (PPT), range of motion and disability in patients with sleep bruxism and myofascial temporomandibular disorders.

Interventions

The muscles were repeatedly perforated by rapidly inserting and partially withdrawing the needle from the myofascial trigger point, eliciting local twitch responses in some insertions

Sponsors

CEU San Pablo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of myofascial temporomandibular disorders * Diagnosis of myofascial trigger point * Diagnosis of sleep bruxism

Exclusion criteria

* insurmountable fear of needles * any systematic joint or muscle disease * bleeding disorders or * prior physical therapy treatment

Design outcomes

Primary

MeasureTime frame
Pain: visual analog scale, ranging from 0mm (no pain) to 100mm (worst imaginable pain).1 week
Pressure pain sensitivity: mechanical pressure algometer.1 week
Range of motion: distance between the upper and lower central dental incisors was measured with a millimeter ruler.1 week

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026