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Clinical Trials in Turkey / NCT07439679
Recruiting Observational

Preoperative Anxiety and Its Impact on Intraoperative Hemodynamics and Postoperative Pain, Edema, and Trismus in Orthognathic Surgery

NCT07439679 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-02-01
Last updated
2026-02-27

Condition(s) studied

Dentofacial Deformities

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * Previous orthognathic surgery * History of maxillofacial trauma * History of radiotherapy or chemotherapy in the head and neck region * Presence of psychiatric disorders or current use of psychiatric medications * Chronic systemic disease affecting bone metabolism or wound healing * Active smoking or substance abuse * Pregnancy or lactation * Incomplete questionnaire responses * Inability to attend follow-up visits

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul Medipol University Hospital Istanbul Turkey (Türkiye) Recruiting

More Istanbul Medipol University Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07439679 on ClinicalTrials.gov ↗ ← All trials in Turkey