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Population Pharmacokinetics and Clinical Individual Dosage Regimen of Propofoll Injection

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03422315
Enrollment
60
Registered
2018-02-05
Start date
2018-09-03
Completion date
2021-09-30
Last updated
2021-06-09

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

Conditions

General Anesthesia

Keywords

Propofol, Population pharmacokinetics, Individualized administration

Brief 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.

Detailed 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.

Interventions

DRUGPropofol

injection;2mg/kg;single-dose

Sponsors

Zhongyuan Xu
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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.).

Design outcomes

Primary

MeasureTime frameDescription
BIS210minbispectral index monitoring

Countries

China

Contacts

Primary Contactzhongyuan xu, Ph.D.
nfyygcp@126.com13926186470
Backup Contactwanwen cao, master
nfyygcp@126.com13631304126

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026