ClinicalTrials.Veeva

Menu

A Study on Central Transport Characteristics of Flurbiprofen Axetil in Elderly Patients

Y

Yi Feng, MD

Status

Unknown

Conditions

Flurbiprofen Axetil
Anesthesia, Spinal
Aged
Cerebrospinal Fluid

Study type

Observational

Funder types

Other

Identifiers

NCT04128410
2019PHB169-01

Details and patient eligibility

About

The project will apply the methods of clinical observation experiment to study the central transport characteristics of flurbiprofen axetil by detecting S-flurbiprofen and R-flurbiprofen concentrations in cerebral-spinal fluid(CSF) after intravenous injection of flurbiprofen axetil in elderly patients.

Full description

The patients undergoing spinal anesthesia for lower extremity surgery will be studied. Flurbiprofen axetil 100mg will be injected intravenously. CSF 1ml and blood 2ml will be obtained simultaneously every 5 minutes after intravenous injection in 50 min( T1~T10).CSF and blood samples will be used to detected S-flurbiprofen and R-flurbiprofen concentrations by using Liquid Chromatography-Mass Spectrometry. And the CSF/blood S-flurbiprofen and R-flurbiprofen concentrations ratio were calculated.

Enrollment

77 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients undergoing lower extremity surgery under spinal or combined spinal-epidural anesthesia will be selected.

Exclusion criteria

  • asthma, liver insufficiency, renal insufficiency, peptic ulcer, allergy to NSAIDs, and a history use of NSAIDs within two weeks before operation.

Trial design

77 participants in 10 patient groups

T1
Description:
At 5 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T2
Description:
At 10 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T3
Description:
At 15 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T4
Description:
At 20 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T5
Description:
At 25 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T6
Description:
At 30 minutes after flurbiprofen axetil injected intravenously, 14 patients' samples were required to be collected,including 7 younger patients
T7
Description:
At 35 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T8
Description:
At 40 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T9
Description:
At 45 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected
T10
Description:
At 50 minutes after flurbiprofen axetil injected intravenously, 7 aged patients' samples were required to be collected

Trial contacts and locations

1

Loading...

Central trial contact

Han Yao; Yi Feng, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems