Study Design Number of patients Treatment Comparator Mean followup Primary outcome Results Adverse events Nardone et al., 1999 [16 ] Prospective cohort study 17 Octreotide 100 g every 8 hours for 6 months Pretreatment 12 months Hemoglobin levels, blood transfusions Effective Not reported Orsi et al., 2001 [17 ] Case series 3 OCT-LAR 20 mg monthly for 12 months Pretreatment 16 months Hemoglobin levels, blood transfusions, bleeding episodes Effective None Junquera et al., 2007 [19 ] Prospective cohort study 32 Octreotide 50 g every 12 hours for 12–24 months Placebo arm of another study 13 months Acute or chronic bleeding, fecal occult blood, iron deficiency anemia Effective Diarrhea (30%) Abdominal pain (10%) Cholestasis (10%) Hyperglycemia (10%) Hypertriglyceridemia (6.6%) Cerebrovascular accidents (3.3%) Scaglione et al., 2007 [13 ] Prospective cohort study 13 OCT-LAR 10 mg monthly for 12 months Pretreatment 33 months Hemoglobin levels, blood transfusions, fecal occult blood Effective Mild diarrhea (1/13) Brown et al., 2010 [20 ] Meta-analysis 62 Octreotide or OCT-LAR, various doses Placebo arm of another study Various Clinical response to treatment, blood transfusions Effective Not reported Bon et al., 2012 [21 ] Prospective cohort study 15 OCT-LAR 20 mg monthly or lanreotide 90 mg monthly for more than 6 months Pretreatment 14 months Hemoglobin levels, blood transfusions, bleeding episodes Effective Not reported Salgueiro et al., 2014 [22 ] Retrospective cohort study 16 OCT-LAR 10–20 mg monthly for at least 12 months Pretreatment 12 months Blood transfusions, hospital admissions Effective Gallstones (1/16 receiving OCT-LAR 20 mg) Splenic infarct (1/16 receiving OCT-LAR 20 mg) Nardone et al., 2014 [23 ] Retrospective cohort study 98 OCT-LAR 20 mg for 6 months Pretreatment 78 months Hemoglobin levels, blood transfusion, hospital admissions Effective Self-limiting diarrhea Impaired glucose tolerance (1%) Cholestasis (1%)