Osteotomy Clinical Trials

Clinical trials related to Osteotomy Procedure

The Effect of Preoperative Anxiety Levels on Intraoperative Hemodynamic Parameters and Postoperative Edema, Pain, and Trismus in Patients Undergoing Bimaxillary Orthognathic Surgery: A Prospective Observational Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study aims to investigate the relationship between preoperative anxiety and intraoperative hemodynamic changes, as well as postoperative pain and facial edema, in patients undergoing orthognathic surgery. Orthognathic surgery is a corrective jaw surgery performed to treat dentofacial deformities. Although the procedure improves functional and aesthetic outcomes, patients may experience significant anxiety before surgery. Elevated anxiety levels may influence physiological responses during the operation and may affect postoperative recovery. In this study, preoperative anxiety levels will be evaluated using validated assessment scales prior to surgery. During the intraoperative period, hemodynamic parameters such as heart rate and blood pressure will be recorded. After surgery, postoperative pain and facial edema will be assessed using standardized clinical evaluation methods. The objective of this research is to determine whether higher levels of preoperative anxiety are associated with changes in intraoperative hemodynamic stability and increased postoperative discomfort. The findings may contribute to improved perioperative management strategies and enhanced patient care in orthognathic surgery.

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

• ASA physical status I or II

• Patients scheduled for bimaxillary orthognathic surgery (Le Fort I osteotomy and bilateral sagittal split ramus osteotomy)

• Ability to understand and complete the STAI questionnaire

• Provision of written informed consent

Locations
Other Locations
Turkey
Istanbul Medipol University Hospital
RECRUITING
Istanbul
Contact Information
Primary
Merve Gaye Akgök, DDS
merve.akgok@std.medipol.edu.tr
+905064571329
Time Frame
Start Date: 2025-02-01
Estimated Completion Date: 2026-04
Participants
Target number of participants: 45
Treatments
Low Anxiety Group
Participants with STAI-I score ≤36 undergoing bimaxillary orthognathic surgery.
High Anxiety Group
Participants with STAI-I score ≥46 undergoing bimaxillary orthognathic surgery.
Related Therapeutic Areas
Sponsors
Leads: Istanbul Medipol University Hospital

This content was sourced from clinicaltrials.gov