The Impact of Lubiprostone on Mucus Secretion in Asymptomatic Volunteers and Patients With Chronic Constipation
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Change of Mucus and Mucin Secretion in Patients With Chronic Constipation and in Controls.
研究概览
简要总结
The investigators hypothesize that the symptoms of chronic constipation in some patients are developed due to diminished production and secretion of the alimentary tract mucus resulting in poor lubrication.
Therefore, the investigators assume that administration of lubiprostone may restore this lubrication impairment by stimulation of mucus production and secretion within the gastrointestinal tract.
详细描述
Specific Aim 1. To test the effect of Lubiprostone, 24 mcg twice a day (BID) for 1 week, on gastric mucus production in 20 asymptomatic volunteers and 20 patients with chronic constipation in basal conditions (primary outcome).
Specific Aim 2. To explore the effect of Lubiprostone, 24 mcg twice a day (BID) for 1 week, on gastric mucus production in 20 asymptomatic volunteers and 20 patients with chronic constipation during stimulation of gastric secretion with pentagastrin, mimicking the meal-stimulated conditions (primary outcome).
Specific Aim 3. To address the influence of Lubiprostone, 24 mcg twice a day (BID) for 1 week, on gastric mucin production, the major component of mucus, in 20 asymptomatic volunteers and 20 patients with chronic constipation in basal conditions (primary outcome).
Specific Aim 4. To test the influence of Lubiprostone, 24 mcg twice a day (BID) for 1 week, on gastric mucin production, the major component of mucus, in 20 asymptomatic volunteers and 20 patients with chronic constipation during stimulation of gastric secretion with pentagastrin, mimicking the meal-stimulated conditions (primary outcome).
Specific Aim 5. To explore the impact of Lubiprostone, 24 mcg twice a day (BID) for 1 week, on viscoelasticity of gastric mucus in 20 asymptomatic volunteers and 20 patients with chronic constipation in basal conditions (secondary outcome).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •18-65 years of age
- •Capable of and willing to give informed consent, and willing to comply with all study requirements
排除标准
- •Pregnancy or lactation
- •Subjects unwilling to practice adequate contraception throughout the screening period through 14 days after study termination
- •Illegal use of illegal drugs
- •Regular consumption of 2 or more drinks of alcohol per day
- •Chronic non-steroidal anti- inflammatory drugs (NSAID) use
- •Chronic use of H2 receptor antagonists or Proton Pump Inhibitors (PPIs) within 14 days prior to screening
- •History of gastric of duodenal ulcer or chronic non-ulcer dyspepsia
- •Positive Helicobacter pylori (H. pylori) serology
- •Patients with Chronic Constipation:
- •Inclusion Criteria:
- •Age 18-65
- •At least 6 months history of constipation. Constipation defined as: a. Less than three complete spontaneous bowel movements per week and one or more of the following: i) At least 25% of stools are very hard and/or hard stools ii) Sensation of incomplete evacuation following at least 25% of bowel movements iii) Straining on at least 25% of defecations The above criteria are only applicable to spontaneous bowel movements. Patients who have no spontaneous bowel movements (bowel movements are preceded by laxative intake) are considered constipated and are eligible for this study
- •For patients >= years of age, normal colonic anatomy as documented by colonoscopy, double-contrast barium enema, or flexible sigmoidoscopy performed within the previous 5 years
- •Exclusion Criteria
- •Pregnancy or lactation
- •Subjects unwilling to practice adequate contraception throughout the period of screening through 14 days after study termination
- •Use of laxatives 3 days immediately prior to randomization (except fiber or bulking agents)
- •Use of any of the following drugs within 3 days prior to randomization a) Prokinetic agents (tegaserod, domperidone, cisapride, metoclopramide, erythromycin, b) Medications containing opiates c) Antispasmodic (e.g. atropine, hyoscyamine, scopolamine, glycopyrrolate)
- •Use of illegal drugs
- •Regular consumption of 2 drinks of alcohol per day
- •Chronic NSAIDs use
- •Chronic use of H2 receptor antagonist or PPIs within 14 days prior to screening
- •History of gastric or duodenal ulcer, Inflammatory bowel disease (IBD), or chronic non-ulcer dyspepsia
- •Diabetes mellitus (DM) type 1
- •Parkinson's disease
- •Existence of any medical condition that requires chronic therapy
- •Positive H. pylori serology
研究组 & 干预措施
Lubiprostone 24 mcg Twice a day
Both controls and patients with chronic constipation will receive 1 week of therapy with lubiprostone and one week of placebo.
干预措施: lubiprostone (Drug)
Placebo
Both controls and patients with chronic constipation will receive placebo pills twice daily for one week in cross over design
干预措施: placebo (Drug)
结局指标
主要结局
Change of Mucus and Mucin Secretion in Patients With Chronic Constipation and in Controls.
时间窗: Measured after 1 week of lubiprostone and 1 week of placebo with 1 week of washout period in between.
The rate of mucus and mucin secretion(mg/hr) will be measured in gastric juice aspirated in basal conditions and during stimulation with pentagastrin after 1 week of therapy with lubiprostone (Active Comparator) and compared with 1 week of placebo administration (Placebo Comparator).
次要结局
- Change in Viscoelasticity of Gastric Secretion in Controls and Patients With Chronic Constipation.(Measured after 1 week of lubiprostone therapy and compared to 1 week of placebo with 1 week of washout in between.)
研究者
Jerzy Sarosiek
Professor of Medicine, Associate Chairman for Research, Internal Medicine Department
Texas Tech University Health Sciences Center, El Paso