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临床试验/NCT02372188
NCT02372188Unknown不适用

Effect of Caffeine With and Without a Bitter Masking Compound on Gastric pH, Taking Into Account the Effect on Satiety Hormones in Blood Plasma and on Food Intake

University of Vienna2 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2013年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
25
试验地点
2
主要终点
Change of the intragastral pH determined by the Heidelberg Detection system

研究概览

简要总结

The purpose of this study is to elucidate whether bitter taste induced by the bitter compound caffeine and the reduction of bitter taste by addition of the bitter masking compound Homoeriodictyol sodium salt (HED) influence gastric acid secretion, subjective feelings of hunger, ad libitum food intake and satiating hormones in healthy volunteers.

详细描述

The influence of 125 mL water, 150 mg caffeine/125 mL water, 30 mg HED/125 mL water or the combination of 150 mg caffeine + 30 mg HED/125 mL water on the gastric pH on different test days was investigated. Prior to the intervention, the trial subjects had to fast from food and liquid for 10 h, except for 200 mL of tap water that were allowed during this time period. During the experiment, the subjects remained in a supine left-sided position.

For the non-invasive measurement of the gastric pH, the Heidelberg Detection System (Heidelberg Medical Inc., USA) was used which has been successfully used in our working group.

This system consists of a pH-sensitive capsule (called a Heidelberg capsule), with a length of 2 cm, that has to be swallowed and contains a miniature radio transmitter. This system allows the detection of the actual gastric pH of the volunteer over a specific time period [Liszt et al 2012, Rubach et al. 2014].

Prior to each test, Heidelberg capsules were activated for 5 min in a 0.9% sterile NaCl solution and calibrated using two calibration points, pH 1 and 7. Afterward, the subjects swallowed the capsule lay down on the left side. The capsule sends a signal to a transceiver, which has to be placed on the abdomen of the volunteer. The transceiver sends the signal to the recorder connected to a computer. The data can be collected and shown as a gastrogram on the computer screen, where the pH is drawn over time. When the intragastric pH was constant between pH 0.5 and 2.5 for at least 3 min, the capsule was considered to be in the stomach. Afterward, each trial started with the administration of 5 mL of a saturated sodium bicarbonate solution (NaHCO3). This alkaline challenge triggers a rise in gastric pH between around pH 6 to 7 and subsequently leads to the secretion of stomach acid by the parietal cells. The test solutions were administered 5 minutes after or 30 min before the alkaline challenge.

Reacidification time as well as the time until start of the reacidification has been analyzed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Single (Participant)

入排标准

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

入选标准

  • good general state of health
  • sensorically untrained
  • BMI: 19 - 26 kg/m2

排除标准

  • gastro-intestinal disease or discomfort,
  • metabolic diseases,
  • H.pylori infection,
  • increased sensibility towards caffeine,
  • intake of antibiotics in the last 2 months,
  • medication except for oral contraceptives,
  • drug- or alcohol-abuse,
  • heart disease, high blood pressure,
  • pregnancy

结局指标

主要结局

Change of the intragastral pH determined by the Heidelberg Detection system

时间窗: recorded over a time period from 1 - 60 min

次要结局

  • Food intake(after the gastric pH measurement on each testing day the subjects are served an ad libitum breakfast, and they have an open time frame how long they want to eat, max. 1 hour is anticipated)
  • Change of plasma levels of Serotonin, Ghrelin, PYY and GLP-1(Plasma are taken at two time points before and after the gastric pH measurement during a time period between 15 - 60 min)
  • subjective feelings of hunger are recorded by means of visual analog scales (VAS)(subjects are asked to fill the VAS out immediately before and after the gastric pH measurement, max. 2 min is anticipated)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Univ.-Prof. Dr. Veronika Somoza

Univ.-Prof. Dr.

University of Vienna

研究点 (2)

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