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临床试验/NCT05845931
NCT05845931已完成不适用

Sex Differences in Berberine Pharmacokinetics in Healthy Volunteers - BERKI-2

University Medicine Greifswald1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年5月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
Berberine plasma concentration women vs. men

研究概览

简要总结

The influence of genetic variants of the CYP2D6 enzyme and the Organic Cation Transporter 1 on the kinetics of berberine (BERKI-1) has recently been studied. By chance, a significant sex difference was observed independent of the genetic variant. The Area under the curve of berberine in women compared to men was about three times higher, and the difference was statistically significant

The aim of BERKI-2 is to confirm the sex difference in an independent second study. In addition, influences of sex hormones on berberine kinetics in women will be studied.

As in BERKI-1, time-dependent blood and urine samples will be collected after a single berberine dose. By measuring berberine metabolites by Liquid Chromatography and Mass-spectrometry standard kinetic parameters e.g., AUC0-24, Cmax, Tmax will be calculated. Age-matched healthy women (n = 15) and men (n = 15) will be enroled.

详细描述

A single dose of 1000 mg berberine will be administered in two capsules with 250 ml of still water in the overnight fasting condition at 8 a.m.. A total of 11 blood samples will be taken at defined time points (baseline, 1; 1.5; 2; 3; 4; 5; 6; 8; 10; 24; h). At each time point, blood will be collected in 2x 7.5 ml tubes for collecting serum and plasma samples to determine berberine concentrations. Another serum sample will be obtained at baseline from women only to determine estradiol, progesterone, luteinizing hormone and follicle stimulating hormone to characterize the first and second phase of the cycle.

Every hour, participants will drink 100 ml of sparkling water to stimulate intestinal peristalsis and promote transport of the capsule. Volunteers are asked to stay in bed during the first four hours but are then allowed to move freely within the Clinical Research Unit. After 2 h, participants may drink a cup of tea or coffee and after 4 h they will be served a meal. Urine will be collected during the first 10 h after administration. Between 2 and 4 p.m., measuring body composition by bioelectrical impedance analysis (BIA) will be peformed to obtain fat mass and fat free mass (total and percentage) and body water. We use the seca mBCA 525 scale.The participants will stay in the Clinical Research Unit of the Institute of Pharmacology for the first 10 h after administration.

Women will undergo this treatment twice at least one week apart. Once in the first half (between days 4-10 after start of menstrual bleeding) and once in the second half (between days 20-26 after start of menstrual bleeding) of their menstrual cycle. The first day of menstrual bleeding marks day 1 as a reference.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

盲法说明

This Study will be an open label study. Participants will be selected from an existing database of our Institute.

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •wild type genotypes for CYP2D6 and Organic Cation Transporter 1
  • •understands the study purpose and design
  • •contractually capable and provides signed informed consent form
  • •healthy condition or mild and/or well treated forms of allergies, asthma, hypertension, and orthopaedic diseases
  • •no regular use of more than 2 drugs

排除标准

  • •volunteers who have already participated in BERKI-1
  • •BMI <18 kg/m2 and >35 kg/m2
  • •disorders of sex hormone regulation, hormone treatments
  • •women: menopause,known pregnancy or lactation period, positive urine pregnancy test at screening and at visits, oral contraceptives, depot contraceptives, or hormone-re-leasing intrauterine devices
  • •anaemia (haemoglobin < 13 g/dl (8,07 mmol/l) in men or < 12 g/dl (7,45 mmol/l) in women
  • •elevated liver function tests (> 2x ULN)
  • •reduced renal function (eGFRMDRD < 60 ml/min/1,7m2)
  • •psychiatric disease or drug dependency at time of visit
  • •use of recreational drugs more than twice a week
  • •poor venous conditions that make it impossible to place a peripheral venous catheter

研究组 & 干预措施

men

Active Comparator

The participants are selected to achieve best matching according to sex, age, BMI, alcohol consumption and smoking between arm 1 and arm 2.

干预措施: Berberine (Dietary Supplement)

woman

Active Comparator

The participants are selected to achieve best matching according to sex, age, BMI, alcohol consumption and smoking between arm 1 and arm 2.

干预措施: Berberine (Dietary Supplement)

结局指标

主要结局

Berberine plasma concentration women vs. men

时间窗: day 1

Difference in berberine plasma concentrations expressed as Area under the Curve between women and men.

次要结局

  • Berberine plasma concentrations durig first and second half of the menstrual cycle(day 1)

研究者

发起方
University Medicine Greifswald
申办方类型
Other
责任方
Principal Investigator
主要研究者

Stefan Engeli, MD

Prof. Dr. med Stefan Engeli

University Medicine Greifswald

研究点 (1)

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