Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 1:33 AM
Ignite Modification Date:
2025-12-25 @ 1:33 AM
NCT ID:
NCT06900894
Brief Summary:
This study investigates the effectiveness of Platelet-Rich Fibrin (PRF) and Kinesio Taping in reducing postoperative pain, edema, and improving recovery following impacted third molar surgery. A prospective, randomized clinical trial was conducted with 44 patients aged 18-35 years. Patients were assigned to three groups: (1) PRF applied locally to the extraction socket, (2) Kinesio Taping applied postoperatively and removed on the third day, and (3) a control group receiving standard postoperative care. Postoperative outcomes were assessed on days 3 and 7, including pain levels, edema, and quality of life. This study aims to evaluate PRF and Kinesio Taping as non-pharmacological adjuncts in oral and maxillofacial surgery.
Detailed Description:
This study investigates the effectiveness of Platelet-Rich Fibrin (PRF) and Kinesio Taping in postoperative management following impacted mandibular third molar surgery. Postoperative complications, such as pain and edema, are commonly observed and may impact patient comfort and recovery. This study aims to evaluate the feasibility of two non-pharmacological approaches-PRF and Kinesio Taping (Elastic Bandaging)-in postoperative care.
A total of 44 patients aged 18-35 years participated in this prospective, randomized clinical trial. Patients were assigned to one of three groups:
PRF Group: Platelet-rich fibrin (PRF) was applied locally into the extraction socket.
Kinesio Taping Group: An elastic bandage was applied postoperatively to the surgical area and removed on the third day.
Control Group: Standard postoperative care was provided with no additional intervention.
Postoperative evaluations were conducted on the 3rd and 7th days. The measured parameters included:
Edema: Measured using anthropometric techniques.
Pain: Assessed with the Numerical Rating Scale (NRS).
Quality of Life: Evaluated using the Oral Health Impact Profile-14 (OHIP-14).
This study aims to assess the feasibility of PRF and Kinesio Taping in postoperative management.
Study:
NCT06900894
Study Brief:
Protocol Section:
NCT06900894