Health Condition 1: K088- Other specified disorders of teethand supporting structures
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patient willing to participate in study. 2.Patients in the age group of 18 -60 years. 3.Patients diagnosed with TMJ arthralgia and intra articular TMJ disorders as given by DC TMD criteria. 4.Patients with VAS score 5 or more pre-operatively
Exclusion criteria
Exclusion criteria: 1.Patients having systemic diseases in which duloxetine is contraindicated. 2.Patients with coagulation disorders. 3.Allergic reaction to local anesthetic agents and duloxetine. 4.TMJ pain following traumatic injury.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the efficacy of arthrocentesis, oral duloxetine alone and combination of arthrocentesis with oral duloxetine in reducing pain in temporomandibular joint disorders.Timepoint: VAS score at day1, day7, 1st month, 3rd month | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the efficacy of arthrocentesis, oral duloxetine alone and combination of arthrocentesis with oral duloxetine in improving the maximum mouth opening in temporomandibular joint disordersTimepoint: Maximum mouth opening at day1, day7, 1st month,3rd month | — |
Countries
India
Contacts
Terna dental college and hospital