Geneva, June 20 -- International Clinical Trials Registry received information related to the study (NCT07020455) titled 'Is the Combine Prolotherapy More Effective Than the Traditional Prolotherapy in Patients With Temporomandibular Joint Hypermobility?' on June 6.
Study Type: Interventional
Study Design:
Allocation: Non-Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Participant).
Primary Sponsor: Karadeniz Technical University
Condition:
Temporomandibular Disorders (TMD)
Temporomandibular Pain
Hypermobility Syndrome (Disorder)
Hypermobility, Joint
Arthrocentesis
Prolotherapy
Intervention:
Drug: prolotherapy solution of 20% dextrose
Recruitment Status: Not recruiting
Phase: Ph...