A Placebo Controlled Trial With Baclofen for the Treatment of GERD Patients With Incomplete PPI Response
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 60
- 主要终点
- efficacy of baclofen on pH-impedance recordings
研究概览
简要总结
Reflux (acid and non-acid) mainly occurs during transient LES relaxations (TLESRs). The gamma-aminobutyric acid (GABA) receptor type B agonist baclofen was shown to inhibit TLESRs, thereby significantly decreasing acid reflux after a meal in healthy controls and in patients with GERD.
The primary objective of this study is to assess the efficacy (assessed by reflux symptom questionnaire and pH-impedance recordings) of baclofen 10mg three times daily vs. placebo in GERD patients with an incomplete response to PPI therapy.
The secondary objective is to assess the predictive value of reflux assessment (by pH-impedance recordings) on the primary outcome.
详细描述
This is a randomized, parallel, double-blind, placebo-controlled, out-patient, single-center study. Eligible subjects will be randomly assigned to receive either oral baclofen 10 mg or placebo t.i.d for a period 4 weeks. After 4 weeks all patients will be given the standard dose of baclofen 10 mg t.i.d. (open label), for another 4 weeks. The b.i.d. PPI therapy will be continued for the entire study duration.
Approximately 90 evaluable subjects with typical GERD symptoms (heartburn and/or regurgitation) will participate in this study and will be randomized on a 1:1 basis: 45 subjects each will be in the placebo and baclofen 10 mg three times daily group. Subjects will be considered to have completed the study if they complete the week 4 visit.
Medication will consist of identically-looking capsules of baclofen or placebo. Patients will take 1 capsule containing 5 mg baclofen with meals t.i.d for 7 days and then 1 capsule containing 10 mg baclofen with meals t.i.d for the remaining 21 days.
Prior to visit 1, all subjects included in the study will undergo a 24 hr pH-impedance study which was requested by the treating physician. This investigation is part of the standard clinical work up and will not be part of the study protocol.
Informed consent is to be signed and dated by the subject before any study related procedures are performed. The date of each visit to the clinic and the date and time of the last dose of test article will be recorded.
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
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •18 - 75 years old
- •History of typical (heartburn/regurgitation) or atypical GERD symptoms during PPI treatment, at least 3 times per week for 12 weeks. Daily intake of PPI treatment 12 weeks prior to inclusion.
- •Sexually active women of child bearing potential participating in the study must use a medically acceptable form of contraception. Medically acceptable forms of contraception include oral contraceptives, injectable or implantable methods, intrauterine devices, or properly used barrier contraception.
- •Subjects must be capable of understanding and be willing to provide signed and dated written voluntary informed consent before any protocol-specific screening procedures are performed.
排除标准
- •Endoscopic signs of severe erosive esophagitis (≥ grade C, Los Angeles classification) on endoscopy performed during PPI treatment in the 6 months prior to screening.
- •Systemic diseases, known to affect esophageal motility.
- •Surgery in thorax or in the upper part of the abdomen.
- •Treatment with baclofen prior to the start of the study.
- •Regular use of medications such as: anticholinergics, tricycle antidepressants.
- •Significant neurological, respiratory, hepatic, renal, haematological, cardiovascular, metabolic or gastroinestinal cerebrovascular disease as judged by the investigator
- •Absence of PPI intake for at least 2 consecutive days in the 2 weeks prior to the screening.
- •Pregnancy or breast feeding.
- •History of poor compliance. History of/or current psychiatric illness that would interfere with ability to comply with protocol requirements or give informed consent. (well-compensated depression is allowed).
- •History of alcohol or drug abuse that would interfere with ability to comply with protocol requirements.
研究组 & 干预措施
baclofen arm
baclofen 10mg tid for 4 weeks
干预措施: Baclofen (Drug)
placebos arm
placebo tid for 4 weeks
干预措施: Placebos (Other)
结局指标
主要结局
efficacy of baclofen on pH-impedance recordings
时间窗: Change from baseline in reflux parameters (total number of reflux episodes) on 24h pH-impedance monitoring at 4 weeks
To assess of baclofen on 24 hour pH-impedance recordings
efficacy of baclofen on reflux symptom questionnaire
时间窗: Change from baseline in ReQuest scores at 4 weeks
To assess the effect of baclofen on reflux symptom questionnaire by ReQuest
次要结局
- Predictive value of the reflux monitoring(Is SAP at baseline predictor of response at 4 weeks)
研究者
Prof Dr Jan Tack
professor
Universitaire Ziekenhuizen KU Leuven