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Effect of dexmedetomidine on cerebral oxygen saturation during hyperventilation during endoscopic sinus surgery

Effect of dexmedetomidine on cerebral oxygen saturation during hyperventilation during endoscopic sinus surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090177
Enrollment
Unknown
Registered
2024-09-25
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic sinusitis

Interventions

Sponsors

General Hospital of Southern Theater Command of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Age range: 18-60 years old; 2) Meets the standards for endoscopic sinus surgery; 3) The patient voluntarily participates in this study and signs a written informed consent form, willing to cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1) Combined hypertension; Diabetes; Patients with a history of taking sedatives for hyperlipidemia; 2) Carotid artery stenosis; Patients with a history of ischemic attacks or cerebral infarction; 3) Patients with a history of taking anticoagulant drugs; 4) When screening for examination, the patient's alanine aminotransferase (ALT) or aspartate aminotransferase (AST) is greater than or equal to 1.5 times the upper limit of the normal value specified by the center, or the endogenous creatinine clearance rate (CCr) is greater than the upper limit of the normal value specified by the center; 5) When screening, the total white blood cell count (WBC) in the patient's blood routine is greater than 10.0X109/L or less than 1.0X09/L; 6) History of any illness that may affect adherence to the protocol (such as severe mental disorders, cognitive impairment, drug abuse or addiction, etc.); 7) Pregnant or lactating women, or those who have the ability to conceive and are unwilling/unable to take effective contraceptive measures; 8) Individuals who are known to be allergic to the ingredients contained in the medication used in this study; 9) Individuals who have participated in any drug clinical trials within the past 6 months prior to screening and examination; 10) Researchers determine that patients who are not suitable to participate in this study;

Design outcomes

Primary

MeasureTime frame
Changes of rSO2 after target controlled infusion of dexmedetomidine;

Secondary

MeasureTime frame
Changes in heart rate after target controlled infusion of dexmedetomidine;Changes in blood pressure after target controlled infusion of dexmedetomidine;Surgical field clarity score;Intraoperative blood loss;PACU residence time;Incidence of postoperative nausea and vomiting;Use of analgesic drugs 24 hours after surgery;

Countries

China

Contacts

Public ContactHuan He

General Hospital of Southern Theater Command of PLA

hlmyf0317@163.com+86 186 0201 9777

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026