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Study on efficacy of joint lavage (arthrocentesis) with and without applied pressure for treatment of temporomandibular joint disorder (internal derangement)

TRIPLE BLIND RANDOMIZED CONTROLLED TRIAL TO STUDY THE EFFICACY OF ARTHROCENTESIS WITH AND WITHOUT APPLIED HIGH PRESSURE IN THE MANAGEMENT OF INTERNAL DERANGEMENT OF TEMPOROMANDIBULAR JOINT. - RAPID-TMJ

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/03/005621
Enrollment
40
Registered
2015-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Internal derangement of Temporomandibular Joint

Interventions

Intervention1: Arthrocentesis of temporomandibular joint under local anesthesia using gravity drip method.: Arthrocentesis of temporomandibular joint under local anesthesia using gravity drip method.

Sponsors

Dr Akilesh R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: RDC/TMD version 1.0 Group II diagnosis

Exclusion criteria

Exclusion criteria: Exclusion Criteria 1. Use of steroid medications. 2. Currently under any other pain medications which could not be stopped for atleast 3 days. 3. Presently using an intra-oral appliance (covering the occlusal surface of any tooth) 4. Presence of any traumatic injury or other clinical problems requiring urgent care. 5. History of trauma and/or surgery to the TMJ or mandible or to any facial bones. 6. Infection in the tissues over the site to be punctured (such as an abscess or cellulitis), adjacent osteomyelitis, uncontrolled coagulopathy or suspected / proved pathology at local site. 7. Significant physical, medical or psychiatric illness or impairment which would preclude ability to comply with study protocols. 8. Patients unwilling to provide signed, informed consent for inclusion in the study. 9. Presence of concomitant non-TMD related causes of pain (ENT, neurological and/or dental causes of pain)

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS) measured by the standard 100 mm VAS scaleTimepoint: 1 week 3 months 6 months

Secondary

MeasureTime frame
Increase in Mandibular function as measured by a decrease in JLFS-8 scoreTimepoint: After 1 week End of 3 months End of 6 months;Unassisted Pain Free Mouth Opening (PFMO) - Interincisal mouth opening measured by a scaleTimepoint: After 1 week End of 3 months End of 6 months

Countries

India

Contacts

Public ContactAkilesh Ramasamy

Nair Hospital Dental College, Mumbai

drnnandrade@yahoo.co.in

Outcome results

None listed

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