Assessment of Chronic Pain Predictors Following Surgical Removal of Mandibular Third Molars

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

Pain is the most common complication following surgical removal of an impacted mandibular third molar. Several risk factors may increase the intensity and duration of pain following removal of mandibular third molars. Acute postoperative pain can transcript into postoperative chronic pain without an explainable reason or a specific risk factor. The use of advanced platelet-rich fibrin in the extraction socket following surgical removal of mandibular third molar have diminished the intensity and duration of acute postoperative pain and facilitated improved wound healing. The objective of the present study is therefore to identified specific risk factors and predictors for developing postoperative chronic pain following surgical removal of mandibular third molars with or without advanced platelet-rich fibrin applied in the extraction socket using epigenetic modulation.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Age ≥ 18 years.

• Presence of a semi- or fully impacted mandibular third molar.

• Indication for surgical removal of mandibular third molar.

Locations
Other Locations
Denmark
Department of Oral and Maxillofacial surgery, Aalborg University Hospital
RECRUITING
Aalborg
Time Frame
Start Date: 2024-01-10
Estimated Completion Date: 2025-12-01
Participants
Target number of participants: 80
Treatments
Active_comparator: With advanced platelet-rich fibrin in the ekstraction socket
Right or left side of the mandible
Placebo_comparator: Without advanced platelet-rich fibrin in the ekstraction socket
Right or left side of the mandible
Related Therapeutic Areas
Sponsors
Collaborators: Aalborg University
Leads: Aalborg University Hospital

This content was sourced from clinicaltrials.gov