跳至主要内容
临床试验/NCT00398801
NCT00398801已完成不适用

Gastroparesis Registry

Johns Hopkins Bloomberg School of Public Health7 个研究点 分布在 1 个国家目标入组 591 人开始时间: 2006年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
591
试验地点
7

研究概览

简要总结

The Gastroparesis Registry (GpR) is an observational study to clarify the epidemiology, natural history, clinical course, and other outcomes of gastroparesis.

详细描述

The Gastroparesis Registry (GpR) is an observational study to clarify the epidemiology, natural history, clinical course, and other outcomes of gastroparesis. The Gastroparesis Registry will also provide a resource to inform the development of clinical trials and ancillary studies of the epidemiology, etiology, pathophysiology, and impact of gastroparesis.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Symptoms of gastroparesis of at least 12 weeks duration (do not have to be contiguous) with varying degrees of nausea, vomiting, abdominal pain, early satiety, post-prandial fullness,
  • Completion of a 4-hour scintigraphic low fat Egg Beaters gastric emptying study
  • Patients with either or both abnormal 2 hour (>60% retention) and 4 hour (>10% retention) gastric emptying will be enrolled and classified as definite gastroparesis (Gp)
  • Patients with normal gastric emptying, but with symptoms of gastroparesis may be enrolled and classified as possible gastroparesis or gastroparesis-like with normal gastric emptying (GLNGE)
  • Age at least 18 years at initial screening visit
  • Ability and willingness to participate in follow-up

排除标准

  • Inability to comply with or complete the gastric emptying scintigraphy
  • Presence of other conditions that could explain the patient's symptoms:
  • Pyloric or intestinal obstruction
  • Active inflammatory bowel disease
  • Eosinophilic gastroenteritis
  • Neurological conditions such as increased intracranial pressure, space occupying or inflammatory/infectious lesions
  • Acute liver failure
  • Advanced liver disease (Child's B or C)
  • Acute renal failure
  • Untreated chronic renal failure (serum creatinine >3 mg/dL)
  • Total or subtotal gastric resection (patients with prior fundoplication or postvagotomy gastroparesis after pyloroplasty or antrectomy with Billroth I, Billroth II, or Roux-en-Y gastrojejunostomy will be eligible for enrollment)
  • Any other plausible structural or metabolic cause
  • Any other condition, which in the opinion of the investigator would interfere with study requirements
  • Inability to obtain informed consent

研究者

申办方类型
Other
责任方
Sponsor

研究点 (7)

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