Endoscopic Evaluation for Iron Deficiency Anemia in Patients on Antithrombotic Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorCentre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec

About this trial

This is a single-center, randomized pilot study evaluating the feasibility and safety of two management strategies for patients on antithrombotic therapy who present with obscure gastrointestinal bleeding (OGIB). Participants will be randomized to either repeated endoscopic evaluations or a conservative medical approach with limited testing. The study aims to assess whether conservative management yields similar clinical outcomes and quality of life compared to standard repeated endoscopic procedures. Results will inform the design of a larger trial and address the current lack of guidelines for managing recurrent iron-deficiency anemia in this patient population.

Eligibility criteria

Qualifiers

Adult men and postmenopausal women with iron deficiency anemia, and premenopausal women with iron deficiency anemia and a negative gynecological evaluation;

Patients receiving anticoagulant or antiplatelet therapy

Negative esophagogastroduodenoscopy (EGD), colonoscopy, and capsule endoscopy for gastrointestinal bleeding within six months prior to study enrollment

Willing and able to provide written informed consent

Disqualifiers

Ongoing overt gastrointestinal bleeding

Acute coronary syndrome, acute neurological event, sepsis, or respiratory failure within the past week

Pregnant women

Known gastrointestinal or hematological malignancy

Trial design

Treatments tested in this trial

  • Standard endoscopic evaluation
  • Conservative Medical Management

Treatment groups

20 Participants
are divided into 2 treatment groups