Presence or Absence of blood in the GI lumen Correlating a HemoPill acute measurement with a subsequent endoscopic finding

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Iron Deficiency Anemia
    Gastrointestinal Haemorrhage, Unspecified
  • Age: Between 18 - 99 Years
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Participants are scheduled for endoscopy due to suspicion of UGIB based on clinical and / or laboratory findings
    2. Provide written informed consent
    3. Willingness and ability to participate in the study procedure

You may not be eligible for this study if the following are true:

    1. The inclusion criteria is not met
    2. Contraindications to the use of the HemoPill acute, such as:
      • Known gastrointestinal obstruction, stricture, fistula, or diverticula
      • Dysphagia or other swallowing disorders
      • Pregnancy
      • Incapacity to provide informed consent
      • In patients with cardiac pacemakers and other implanted medical devices

If you are registered as a volunteer, please log in to contact the study team/express interest in this study.

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