Population Pharmacokinetics and Clinical Individual Dosage Regimen of Propofoll Injection

General Anesthesia Clinical Trial

Official title:

Population Pharmacokinetics and Clinical Individual Dosage Regimen of Propofoll Injection in Adult Patients With General Anesthesia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03422315
• Other study ID #: C1033453
• Status: Recruiting
• Phase: N/A
• Start date: September 3, 2018
• Est. completion date: September 2021

Study information

• Verified date: March 2021
• Source: Nanfang Hospital of Southern Medical University
• Contact: zhongyuan xu, Ph.D.
• Phone: 13926186470
• Email: nfyygcp[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Propofol is a widely used sedative anesthetic, but there are large individual differences, which making different patients with different sensitivity to propofol. The aim of this study was to analyze the effects of age, height, body weight, Drinking, metabolic enzymes CYP2B6 and UGT1A9 on Pharmacological effects and pharmacokinetics of propofol, and to provide a reasonable reference for clinical anesthesia patients and evidence for individual dosage regimens.

Description:

Propofol is a widely used sedative anesthetic, but there are large individual differences, which making different patients with different sensitivity to propofol. In recent years, the concept of individualized administration came into being.Individual administration refers to according to the condition of patients,the drug's safety and efficacy, and pharmacokinetics, pharmacodynamics and clinical response ,then gives different dosing regimens for individual patients and promotes the development of rational drug use. Different people have differences metabolism of propofol, reported in the literature, genetic polymorphism, demographic characteristics, combined with drug and other variability factors, all of them will affect the pharmacokinetics and pharmacodynamics of propofol.The aim of this study was to analyze the effects of age, height, body weight, Drinking, metabolic enzymes CYP2B6 and UGT1A9 on Pharmacological effects and pharmacokinetics of propofol, and to provide a reasonable reference for clinical anesthesia patients and evidence for individual dosage regimens.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: September 2021
• Est. primary completion date: September 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• patients aged 18-60 years (including those aged 18 and 60) who underwent gastrointestinal endoscopy;

• weight should not be less than (=) 50kg, not more than (=) 80kg. Body mass index (BMI) = body weight kg / [(height m) 2], in the normal range of 19 to 25;

• American Society of Anesthesiologists (ASA) grading (Appendix I): I or II;

• no heart, liver, lung, kidney, digestive tract, nervous system, mental disorders and other medical history, no blood and metabolic diseases and other medical history, no potential difficulties airway and special past history,

• blood, urine, stool routine, liver and kidney function, blood lipids, ECG, chest X-ray and blood pressure normal, or abnormal but no clinical significance, the researchers believe that can be grouped.

• agree and sign informed consent.

Exclusion Criteria:

• important organs have primary disease;

• persons with mental or physical disabilities;

• those suffering from neurological or mental illness, a history of epilepsy;

• patients with cardiovascular or respiratory insufficiency and hypovolemia;

• obese or those with dyslipidemia;

• hereditary acute porphyria;

• infections, especially those with respiratory and central infections;

• language exchange barriers;

• suspected or indeed a history of alcohol, drug abuse; especially long-term use of non-steroidal anti-inflammatory drugs, opioids, tranquilizers;

• allergies, if the history of drugs or food allergies; or known to propofol, soybeans, peanuts, coconut oil allergy;

• smoking history (smoking = 5 per day);

• 2 weeks before the trial had used all kinds of Chinese and Western medicine;

• the last 3 months of blood donors and test blood donors;

• other circumstances that the researcher thinks can not be grouped (eg, frail, etc.).

Related Conditions & MeSH terms

• General Anesthesia

Intervention

Drug:
• Propofol
injection;2mg/kg;single-dose

Locations

Country	Name	City	State
China	Nanfang Hospital,Southern Medical University	Guangzhou	Guangdong

Sponsors (1)

Lead Sponsor	Collaborator
Zhongyuan Xu

Country where clinical trial is conducted

China, 

References & Publications (4)

Bernard O, Guillemette C. The main role of UGT1A9 in the hepatic metabolism of mycophenolic acid and the effects of naturally occurring variants. Drug Metab Dispos. 2004 Aug;32(8):775-8. — View Citation

Kansaku F, Kumai T, Sasaki K, Yokozuka M, Shimizu M, Tateda T, Murayama N, Kobayashi S, Yamazaki H. Individual differences in pharmacokinetics and pharmacodynamics of anesthetic agent propofol with regard to CYP2B6 and UGT1A9 genotype and patient age. Drug Metab Pharmacokinet. 2011;26(5):532-7. Epub 2011 Aug 23. — View Citation

Khan MS, Zetterlund EL, Gréen H, Oscarsson A, Zackrisson AL, Svanborg E, Lindholm ML, Persson H, Eintrei C. Pharmacogenetics, plasma concentrations, clinical signs and EEG during propofol treatment. Basic Clin Pharmacol Toxicol. 2014 Dec;115(6):565-70. doi: 10.1111/bcpt.12277. Epub 2014 Jul 19. — View Citation

Takahashi H, Maruo Y, Mori A, Iwai M, Sato H, Takeuchi Y. Effect of D256N and Y483D on propofol glucuronidation by human uridine 5'-diphosphate glucuronosyltransferase (UGT1A9). Basic Clin Pharmacol Toxicol. 2008 Aug;103(2):131-6. doi: 10.1111/j.1742-7843.2008.00247.x. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	BIS	bispectral index monitoring	210min