NCT00101985已完成2 期
An Eight-week, Randomized, Double-blind, Placebo-controlled, Dose-ranging Study to Evaluate Efficacy and Safety of Talnetant in Subjects With Irritable Bowel Syndrome
适应症
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 741
- 试验地点
- 135
- 主要终点
- Determine whether talnetant provided adequate relief from IBS pain and discomfort for at least one of three talnetant dose groups compared with placebo and to determine the safety and tolerability of talnetant in subjects with IBS.
研究概览
简要总结
This study will evaluate the effectiveness and safety of the investigational drug talnetant in treating subjects with irritable bowel syndrome (IBS).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects will be required to conduct self-assessments of their IBS symptoms using a touch-tone telephone system for the duration of the study (15 weeks).
- •Must be diagnosed with IBS consistent with the Rome II criteria.
- •Must have normal results from a colonic procedure within 2 years of randomization.
- •Must have conducted self-assessments on at least 12 days and have a documented average IBS pain or discomfort score of greater than or equal to 1.5 during the two-week screening phase.
排除标准
- •Self-assessment of no stool for 7 days during the two-week screening phase.
- •Clinically significant abnormal laboratory tests.
- •Current evidence or history of various conditions, comorbidities, or surgeries such as Irritable Bowel Disease (IBD), gastrointestinal surgeries, and diverticulitis.
- •Inability to use the touch-tone telephone system.
- •Hypersensitivity to quinolone antibiotics or quinolone derivatives.
- •Diagnosis of a psychiatric disorder within the past 2 years and not on a stable dose of medication for at least 6 months.
- •Women who are pregnant, breast feeding, or planning to become pregnant during the study.
- •Permitted medications: The subject is allowed to take any of the following medications, provided they maintain a stable dose for at least 30 days prior to the Screening visit and throughout the remainder of the study:
- •Antidepressants, except REMERON
- •Antihypercholesterolemics
- •Iron supplements
- •Bulking agents
- •Fiber supplement
- •Thyroid replacement therapy (levothyroxine)
- •Antipsychotics
- •Cox-2 inhibitors (CELEBREX)
- •Prohibited medications: Subjects must stop taking any medications they are taking to treat their IBS symptoms and must not have taken any of the prohibited medications at least 7 days prior to the Screening visit and must remain off these medications for the duration of the study.
- •Anticholinergics (dicyclomine, hyoscyamine, propantheline)
- •Cholinomimetic (bethanechol, pyridostigmine, tacrine, physostigmine)
- •All narcotics (morphine, codeine, TYLENOL #3, propoxyphene, either alone or in combination)
- •Tramadol hydrochloride (ULTRAM)
- •Colchicine
- •Orlistat (XENICAL)
- •Misoprostol, alone or in combination (ARTHROTEC, CYTOTEC)
- •5-HT3 receptor antagonists (ondansetron, tropisetron, dolasetron, granisetron, mirtazapine, cilansetron, alosetron)
- •Tegaserod (ZELNORM)
- •Gabapentin
- •Antacids containing magnesium or aluminium
- •Antidiarrheal agents
- •Bismuth compounds
- •Prokinetic agents (cisapride, metoclopramide)
- •Sulfasalazine
- •Laxatives
- •Cholestyramine
结局指标
主要结局
Determine whether talnetant provided adequate relief from IBS pain and discomfort for at least one of three talnetant dose groups compared with placebo and to determine the safety and tolerability of talnetant in subjects with IBS.
次要结局
- - Explore response among subgroups IBS. - Evaluate positive treatment effects within bowel subgroups. - Compare treatment groups for global improvement of IBS symptoms. - Improvement of IBS pain or discomfort, Quality of Life.
研究者
研究点 (135)
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