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临床试验/NCT01837030
NCT01837030撤回不适用

Capsule Endoscopy Versus Conservative Therapy for Obscure Gastrointestinal Bleeding

Medical University of South Carolina2 个研究点 分布在 1 个国家开始时间: 2013年3月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Time to first blood transfusion after randomization

研究概览

简要总结

This study is a single center prospective randomized control trial comparing the utility of performing capsule endoscopy compared to conservative management with oral iron therapy as the initial course of action in patients with non-severe obscure occult or obscure overt gastrointestinal (GI) bleeding. The investigators hypothesize that outcomes in patients with non-severe obscure GI bleeding who receive conservative therapy with oral iron will not differ to those on oral iron who undergo capsule endoscopy.

详细描述

Although the American Gastroenterological Association suggests that patients with obscure GI bleeding undergo a capsule endoscopy after a negative esophagogastroduodenoscopy (EGD) and colonoscopy, current recommendations from the British Society of Gastroenterology argue that unless there is an inadequate response to iron therapy, further imaging of the small bowel is probably not necessary. Several studies have demonstrated that this approach is reasonably safe. Furthermore, Laine et al demonstrated that when patients with obscure GI bleeding were randomized to either capsule endoscopy or dedicated small bowel contrast radiography, the rates of further bleeding, measured by subsequent hospitalization and blood transfusion events, were similar between the two groups. No study has randomized patients with obscure GI bleeding to receive capsule endoscopy vs. conservative therapy with oral iron.

This study is a single center prospective randomized control trial comparing the utility of performing capsule endoscopy compared to conservative management with oral iron therapy as the initial course of action in patients with non-severe obscure occult or obscure overt gastrointestinal bleeding. All patients will be recruited in the G.I. clinic, the endoscopy unit, or during inpatient consults after negative upper endoscopy and colonoscopy. The study will be explained to patients who qualify at that time. During this visit, patients will be questioned with regard to lower or upper G.I. symptoms, including abdominal pain, dyspepsia, nausea, vomiting, weight loss, diarrhea, change in stool character, melena and intermittent hematochezia. All patients will be started on standard dose oral iron therapy after informed consent. If the patient is already taking iron supplements, their dose with be adjusted to the standard regimen after informed consent. Patients will then be randomized to undergo capsule endoscopy or not. For patients randomized to undergo capsule endoscopy, all subsequent evaluation and treatment will be determined by capsule findings (i.e. capsule directed management) and standard of care at our institution.

Patients will be followed for 1 year. Follow up lab draws will occur at 1, 3, 6 and 12 months. They will consist of a complete blood count (CBC) and ferritin and can be performed at either the Medical University of South Carolina (MUSC) or an outside facility or office. If performed outside of MUSC, a standard medical records release form will be utilized to obtain the lab information. Patients will be provided with a paper card indicating their date of enrollment in the study. This card will be kept by the patient for the entire 12 month follow up period and will be collected at the end of the follow up period. The card will have an area where the patient can write the date of their first blood transfusion after enrollment. There will also be numerical checkboxes that the patient will check off for each unit of packed red blood cells (RBCs) they receive during the 12 month follow up period. Telephone calls will be made to each patient every 3 months after enrollment to inquire about hospitalizations and bleeding related procedures (including endoscopy, capsule, small bowel radiology, interventional radiology and surgery). Records of these hospitalizations and procedures will be obtained using a standard medical records release form.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

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

  • Adult men and post-menopausal women with iron deficiency anemia and pre-menopausal women with iron deficiency anemia and a negative gynecologic workup or adults with overt GI bleeding as defined by melena or hematochezia with a ≥2 gram drop in hemoglobin after stabilization (Iron deficiency is defined as hemoglobin <13.7 g/dL in men and <12 g/dL in women with serum ferritin level <50 ng/mL). Also, patients with an otherwise unexplained drop in hemoglobin of ≥ 2 g/dL in the setting of hemoccult positive stool
  • Negative EGD and colonoscopy for source of GI bleeding within six months of enrollment into the study.

排除标准

  • Ongoing overt gastrointestinal bleeding requiring ≥4 units of packed RBC's on any given day in the setting of overt bleeding, blood transfusions on separate days (separated by ≥12 hours), or ≥6 units of packed RBC's over the previous 7-day period prior to presentation, in the setting of overt bleeding.
  • Myocardial infarct, acute neurologic event, sepsis, or respiratory failure within the previous 1 week
  • History of small bowel obstruction
  • Pregnant women
  • Prisoners
  • Age less than 18
  • Known GI or hematologic malignancy
  • Achalasia
  • Contraindications to capsule endoscopy (inability to take prep), or felt unsafe to undergo capsule as per study investigators
  • Esophageal stricture that precludes even endoscopic capsule placement
  • History of upper GI or small bowel surgery
  • Inability to take oral iron.
  • Active IV iron use.
  • Alternate source of blood loss (e.g., menorrhagia)
  • Hematemesis sufficient to be the cause of the hemoglobin decline

研究组 & 干预措施

Oral Iron and Capsule Endoscopy

Other

干预措施: Capsule Endoscopy (Device)

Oral Iron and Capsule Endoscopy

Other

干预措施: Ferrous sulfate (Dietary Supplement)

Oral Iron

Other

干预措施: Ferrous sulfate (Dietary Supplement)

结局指标

主要结局

Time to first blood transfusion after randomization

时间窗: 12 month follow up period

Time-to-event analysis. Patients will be provided an index card on which they will record the date of their first blood transfusion after randomization

次要结局

  • Total number of bleeding-related procedures performed after randomization(3, 6, 9, and 12 months)
  • Total number of hospitalizations(3, 6, 9, and 12 months)
  • Mortality(3, 6, 9, and 12 months)
  • Total number of blood transfusions(3, 6, 9, and 12 months)
  • Persistent Iron Deficiency Anemia as measured by ferritin and hemoglobin(1, 3, 6, and 12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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