None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: -Bilateral IMTMs with similar difficulty -Underlying medical conditions well managed
Exclusion criteria
Exclusion criteria: -Autoimmune diseases, hemorrhagic disorders, psychiatric disorders or those suspected of having psychiatric disorders. -History of hypersensitivity to polydeoxyribonucleotide (PDRN) -Pregnant or breastfeeding women -Malignant tumors or those undergoing chemotherapy -Alcohol dependency -Any other individuals inappropriate for participation in the clinical study based on the researcher's judgment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative Pain | — |
Secondary
| Measure | Time frame |
|---|---|
| Pocket Probing Depth;Patient Centered Outcome Questionnaire((Pain, whether additional painkillers were taken, subjectively perceived level of facial swelling, intraoral bleeding, intraoral discomfort, pronunciation, and mouth opening amount are divided into left and right and evaluated by dividing them into never/hardly ever/occasionally/fairly often/very often);pain duration time;Postoperative swelling | — |
Countries
Korea, Republic of
Contacts
Yonsei University, Wonju Severance Christian Hospital