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Enhancing occlusal appliances success- comparing two therapies

A comparative evaluation of the effect of transcutaneous electrical nerve stimulation and ultrasonic therapy by salivary biomarkers and visual analogue scale in patients undergoing treatment for mild to moderate malocclusion with occlusal appliances - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072671
Enrollment
48
Registered
2024-08-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified Health Condition 2: Z464- Encounter for fitting and adjustment of orthodontic device

Interventions

Intervention1: TENS: transcutaneous electrical nerve stimulation will be given at 2 sessions to the patients Control Intervention1: ultrasonic: ultrasonic therapy will be given at 2 sessions to the pa

Sponsors

Dr Simran Chadha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients presenting with mild to moderate malocclusion 2.Patients with no pain or tenderness on palpation of TMJ 3.Patients with no pain on any type of mandibular movement 4.Patients with no reduction in mandibular opening measured inter-incisally 5.Patients with no deviation or deflection of the mandible on opening 6.Patients with no palpable, audible, or symptomatic popping, clicking or crepitation in TMJ mandibular movements 7.Patients should have sufficient occlusal stops 8.Patients with proper oral hygiene 9.Patients with no relevant medical history

Exclusion criteria

Exclusion criteria: 1.Patients with pain in the TMJ before treatment. 2.Patients having reduced mouth opening due to TMJ pathology 3.Symptoms related to disease in other parts of stomatognathic system (eg, toothache, neuralgia etc) 4.Patients having periodontally compromised dentition 5.History of chronic illness 6.Patients with a history of smoking 7.Pain due to systemic diseases (eg, Rheumatoid arthritis etc.) 8.Patients with diagnosed Psychological disorders. 9.Pregnant or lactating women 10. Having an infectious disease known to be transmitted by saliva.

Design outcomes

Primary

MeasureTime frame
visual analogue scale scoreTimepoint: visual analogue scale score will be assessed at 4 weeks and 8 weeks of treatment

Secondary

MeasureTime frame
not applicableTimepoint: not applicable

Countries

India

Contacts

Public ContactShrimant Raman

Manav Rachna Dental College

pankajdhawan@gmail.com9810636814

Outcome results

None listed

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