Hypotensive Anesthesia for Orthognathic Surgery

Orthognathic Surgery Clinical Trial

Official title:

A Comparison of Dexmedetomidine, Nicardipine, and Labetalol to Induce Hypotensive Anesthesia and Their Effects on Surgeon Visibility, Blood Loss, Hemodynamic Parameters, Operation Time, and Adverse Events During Orthognathic Surgery

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06093893
• Other study ID #: H-43663
• Status: Not yet recruiting
• Phase: Phase 4
• Start date: May 2024
• Est. completion date: March 2025

Study information

• Verified date: March 2024
• Source: Boston Medical Center
• Contact: Pushkar Mehra, DMD
• Phone: 617-638-4350
• Email: pushkar.mehra[@]bmc.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The overall objective of this double blinded, randomized controlled trial (RCT) is to compare specific outcomes of three medications (Dexmedetomidine, Nicardipine, and Labetalol) which are routinely used to lower blood pressure used during general anesthesia for orthognathic (jaw) surgery. The outcome measures for the study will be surgical field visibility, estimated blood loss, hemodynamic parameters, operation time, and adverse events. The specific objectives of this study are to compare: 1. Dexmedetomidine, Nicardipine, and Labetalol's effect on the quality of the surgical field. (Primary Outcome) 2. Dexmedetomidine, Nicardipine, and Labetalol's effect on estimated blood loss. 3. Dexmedetomidine, Nicardipine, and Labetalol's effect on hemodynamic parameters including systolic blood pressure, mean arterial pressure, and heart rate. 4. Dexmedetomidine, Nicardipine, and Labetalol's effect on operation time. 5. Dexmedetomidine, Nicardipine, and Labetalol's effect on adverse events. The investigators will evaluate healthy adult male and female patients who require jaw surgery at Boston Medical Center. The anticipated 90 participants will be randomized into three groups: ) A Labetalol group in which the patients receive hypotensive anesthesia with the aid of labetalol, 2) A Nicardipine group in which the patients receive hypotensive anesthesia with the aid of nicardipine, and 3) A Dexmedetomidine group in which the patients receive hypotensive anesthesia with the aid of dexmedetomidine. The time it will take for each individual participant ranges from 1-3 months. This time includes the pre-operative visit, the surgical procedure, a 1-week post-operation visit, and then followed for 30 days post-operatively after which the patient's participation in the study will conclude.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 90
• Est. completion date: March 2025
• Est. primary completion date: March 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult patients undergoing orthognathic surgery [Le Fort I, Surgically Assisted Rapid Palatal Expansion (SARPE), Bilateral Sagittal Split Osteotomy (BSSO), or a combination these surgeries] at Boston Medical Center with Dr. Mehra
• Healthy, American Society of Anesthesiologists (ASA) physical status classification system I or II

Exclusion Criteria:

• Patients on a home beta blocker
• Patients on home calcium channel blocker
• Patients on home alpha 2 agonists
• Patients with an allergy to one or more of the intervention medications
• Does not speak English
• Pregnant patients (this is assessed day of surgery per standard care with a urine pregnancy test)
• Patients who have contraindications to induced hypotensive anesthesia

Related Conditions & MeSH terms

• Hypotension
• Hypotensive Anesthesia
• Orthognathic Surgery

Intervention

Drug:
• Dexmedetomidine
1 mcg/kg will be administered intravenously over 10 minutes; followed by maintenance infusion of 0.2 to 1 mcg/kg/hour.
• Nicardipine
1 mg will be administered intravenously and increase by 0.5-1 mg if the initial dose is ineffective, to a maximum of 15 mg / hour or
• Labetalol
20 - 80 mg will be administered intravenously at 10-minute intervals to maximum of 300 mg;

Locations

Country	Name	City	State
United States	Boston Medical Center	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Boston Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Surgical field visibility	Surgical field visibility will be assessed using the Fromme's scale (0 = no bleeding, virtually bloodless field, 1 = bleeding, so mild it was not even a surgical nuisance, 2= moderate bleeding, a nuisance but without interference with accurate dissection, 3 = moderate bleeding that moderately compromised surgical dissection, 4 = bleeding, heavy but controllable, that significantly interfered with dissection, 5 = massive uncontrollable bleeding). This data will be obtained from the surgeon in the form of an electronic survey, and the mean value will be recorded.	immediately after surgery
Secondary	Estimated blood loss	This outcome will be calculated by the volume in suction minus the volume of irrigating fluid.	immediately after surgery
Secondary	Mean systolic blood pressure during surgery	This outcome will be automatically recorded in the electronic medical record every 5 minutes during surgery.	throughout surgery every 5 minutes
Secondary	Mean arterial pressure	This outcome will be automatically recorded in the electronic medical record every 5 minutes during surgery.	throughout surgery every 5 minutes
Secondary	Mean heart rate	This outcome will be automatically recorded in the electronic medical record every 5 minutes during surgery.	throughout surgery every 5 minutes
Secondary	Operation time	Operation time will be measured from time of first incision to procedure end, as recorded in electronic medical record.	immediately after surgery