Trials / Completed
CompletedNCT07133048
Evaluation of Regional Blocks Efficacy in Orthognathic Surgery
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 72 (actual)
- Sponsor
- Clinical Hospital Center Rijeka · Academic / Other
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
The proposed study, which will be carried out on 72 male and female patients, who have reached bone maturity, are younger than 50 years and underwent orthognathic surgical procedures. Patients will be divided into a study group which will receive a regional block with levobupivacaine and a control group that will receive saline as a placebo. The main hypothesis is that regional analgesia in orthognathic surgery contributes to intraoperative and postoperative analgesia. The aim is to determine the real benefit of regional analgesia in orthognathic surgery and analyze the impact of psychosocial factors on results. Various psychological questionnaires, pain scale and questionnaires for evaluation of postoperative recovery will be used in the research. The results of the research could contribute to a better understanding of regional anesthesia in orthognathic surgery and determine impact of psychosocial factors on pain level and satisfaction with orthognathic surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Levobupivakain 0.25 % | The high tuberosity approach blocks for blockage of II. branch of trigeminal nerve. Standard intraoral approach for inferior alveolar nerve block. |
| PROCEDURE | NaCl 0.9 % | The high tuberosity approach blocks for blockage of II. branch of trigeminal nerve. Standard intraoral approach for inferior alveolar nerve block. |
Timeline
- Start date
- 2020-03-02
- Primary completion
- 2022-09-02
- Completion
- 2023-12-02
- First posted
- 2025-08-20
- Last updated
- 2025-08-20
Locations
1 site across 1 country: Croatia
Source: ClinicalTrials.gov record NCT07133048. Inclusion in this directory is not an endorsement.