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TENS in temporomandibular joint dysfunction

Role of transcutaneous electrical nerve stimulation in temporomandibular joint disorders: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230622058557N1
Enrollment
140
Registered
2023-06-27
Start date
2021-01-01
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Temporomandibular joint disorder: a group of conditions that cause pain and dysfunction in the jaw joint and muscles that control jaw movement.. Temporomandibular joint disorders

Interventions

Intervention 1: Intervention group: TENS group. ATENS machine is a small, battery-operated device that has leads connected to sticky pads called electrodes which were placed in close proximity to the

Sponsors

Armed Forces Institute of Dentistry
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Participants who met specific inclusion criteria were included in the investigation. Individuals between ages of 18 and 65 who had been diagnosed with Temporomandibular Joint Dysfunction (TMD) and were experiencing pain or distress in the temporomandibular joint region met these criteria. Dysfunction of masticatory muscles Restrictive jaw movements at Temporomandibular Joint Clicking sound at Temporomandibular Joint Sensitivity to palpation at Temporomandibular Joint

Exclusion criteria

Exclusion criteria: patients with contraindications for TENS or analgesic use, such as pacemakers, epilepsy, or pregnancy participants who had previously received TENS or analgesic treatment for TMD were excluded severe medical conditions

Design outcomes

Primary

MeasureTime frame
Decrease in Pain as shown by Decrease in VAS Pain Ratings. Timepoint: 1,2,3,4 Weeks after intervention. Method of measurement: Visual Analogue Score (VAS).

Secondary

MeasureTime frame
Functional Impairment- Relief in mouth opening. Timepoint: 2,3,4 Weeks after intervention. Method of measurement: MMO- Millimeter mouth opening.

Countries

Pakistan

Contacts

Public ContactSyeda Mahnoor Fatima

Armed Forces Institute of Dentistry affiliated with National University of Medical Sciences

mahnooorbukhari@gmai.com+92 335 5508126

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026