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Evaluation of postoperative pain from TMJ surgery and dexamethasone infiltration

Evaluation of postoperative pain in patients undergoing joint arthroscopy mandibular temporalis with infiltration of dexamethasone disodium phosphate in different isolates

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-28yb2g
Enrollment
Unknown
Registered
2020-05-27
Start date
2019-09-10
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Diseases of the musculoskeletal system and connective tissue

Interventions

Group A (control
12 participants): without intervention after TMJ atroscopy Group B (12 participants): TMJ infiltration with 2mg of corticosteroids right after TMJ atroscopy, which is performed according to clinical p
Procedure/surgery

Sponsors

Sociedade Beneficente de Senhoras Hospital Sírio-Libanês
Lead Sponsor
Sociedade Beneficente de Senhoras Hospital Sírio-Libanês
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: patients needing surgery; arthroscopic TMJ, temporomandibular disorders with Wilkes stages III and IV (Wilkes 1989) caused any of these pathologies: degenerative joint disease; synovitis; painful hypermobility; recurrent dislocation of disc cause; hypomobility caused by intra- articular; inflammatory arthropathies

Exclusion criteria

Exclusion criteria: skin or joint infection tumors ankylosis diabetic neuropathies; fibromyalgia and / or neuromuscular diseases; multiple sclerosis; also patients allergic to dexamethasone; unilateral TMJ surgery

Design outcomes

Primary

MeasureTime frame
Lower levels of pain in 7 days in groups B and C, verified by visual analog scale, from the finding of an average difference of at least 2 points on the scale (1-10) and with statistical significance

Secondary

MeasureTime frame
Better TMJ function in 7 days in groups B and C, verified by measuring mouth opening (mm), based on the observation of an average difference of at least 15% and with statistical significance, ;Less need for analgesic medications in the postoperative period in groups B and C, verified by collecting information on medication use, based on the observation of an average difference of at least 15% and with statistical significance ;Similar complication rates between all groups, verified by collecting information on complications, based on the finding of statistical equality ;Similar satisfaction levels between all groups, verified by visual analog scale of satisfaction after 30 days of the intervention, from the finding of a statistical equality;Less need for analgesic medications in the postoperative period in groups B and C, verified by collecting information on medication use, based on the observation of an average difference of at least 15% and with statistical significance ;Similar complication rates between all groups, verified by collecting information on complications, based on the finding of statistical equality ;Similar satisfaction levels between all groups, verified by visual analog scale of satisfaction after 30 days of the intervention, from the finding of a statistical equality

Countries

Brazil

Contacts

Public ContactIvan Martins

Sociedade Beneficente de Senhoras Hospital Sírio-Libanês

ivan.sol.m@gmail.com+55 11 975531559

Outcome results

None listed

Source: REBEC (via WHO ICTRP)