Liquid Phase Concentrated Growth Factor Versus Conventional Arthrocentesis in Temporomandibular Disc Displacement
Launched by HORUS UNIVERSITY · Jul 11, 2025
Trial Information
Current as of November 13, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new treatment called Liquid Phase Concentrated Growth Factor (LPCGF) to help people with a jaw joint problem known as temporomandibular disorder (TMD), specifically when the disc inside the joint is out of place. The study will compare LPCGF with a standard treatment called arthrocentesis, which involves flushing the joint to reduce pain and improve movement. The goal is to find out if LPCGF is safe and works well as an alternative treatment for this condition.
Adults between 18 and 45 years old who have a diagnosis of disc displacement in one side of their jaw joint, experience symptoms like pain, clicking sounds, or difficulty opening their mouth fully, and have healthy teeth and jaw alignment might be eligible to join. Participants should not have had surgery or injections in the jaw joint before and must be generally healthy without certain medical conditions. If you join the study, you can expect to receive either the new LPCGF treatment or the standard joint flushing, and your progress will be closely monitored to see how well you improve. This study is not yet recruiting, but it aims to provide helpful information for people looking for better ways to treat jaw joint problems.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Adults aged 18-45 years. 2. Patients scored as (ASA I).9 3. Presence of complete or nearly complete set of natural dentition with Angle class I occlusion. 4. Diagnosed with unilateral involvement of disc displacement, according to the Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD).10 5. Symptoms include one or more of the following: pain, joint sounds, and limited mandibular movement (Maximum Mouth Opening\< 40mm) 6. No prior surgical intervention for TMD. 7. Patient's willingness to participate and follow the study protocol.
- Exclusion Criteria:
- • 1. TMJ pathology related to mechanical deformities 2. Psychiatric problems or presence of systemic diseases that may affect healing (e.g., uncontrolled diabetes, autoimmune disorders, hematologic or neurologic disorders, inflammatory or connective tissue disorders as well as rheumatological or previous infectious diseases, head and neck cancer). 3. Patient unwilling or has contraindication to MRI 4. Previous injections or surgical interventions of the TMJ. 5. Concurrent use of anticoagulants or anti-inflammatory medications within the last 30 days. 6. Pregnant or breastfeeding women. 7. History of trauma or infection in the TMJ region. 8. Allergy to local anesthetics or other components used in the study. 9. Patients diagnosed with (Disc Displacement with reduction with no pain or limited mandibular movements).
About Horus University
Horus University is a leading academic institution dedicated to advancing medical research and education. With a commitment to innovative healthcare solutions, the university actively sponsors clinical trials that aim to enhance treatment methodologies and patient outcomes. By fostering collaboration between researchers, clinicians, and industry partners, Horus University leverages its expertise and resources to conduct rigorous, ethically sound studies that contribute to the scientific community and improve healthcare practices globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Damietta, New Damietta, Egypt
Patients applied
Trial Officials
Mohamed Ali Habib, Teaching Assistant
Principal Investigator
Horus University in Egypt - Faculty of dentistry
Eman AbdElsalam Yousef, Ass. prof
Study Director
Horus University in Egypt- Faculty of dentistry
Ahmed Khalil, lecturer
Study Director
Horus University in Egypt - Faculty of dentistry
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported