Phase
Condition
Holoprosencephaly
Surgery
Anemia
Treatment
Ferric derisomaltose
Ferrous succinate
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria
Age ≥18 years
Received spinal deformity surgery
70 g/L ≤ Hb ≤ 110 g/L at POD1, or Hb at POD1 showed a decrease of
≥20 g/L compared with baseline
- Informed consent was obtained voluntarily
Exclusion Criteria
Women who are pregnant, breastfeeding, or planning to become pregnant.
known serious hypersensitivity to other parenteral iron products
Non-iron deficiency anemia (e.g., hemolytic anemia)
Decompensated liver insufficiency
Coexisting active infection
Drug abuse, including but not limited to opioids, amphetamines, methamphetamine, ketamine, etc.
Other conditions that the investigator considers inappropriate for participation (e.g. deafness, Parkinson's disease, communication disorders, etc.)
Participation in another clinical trial within three months prior to this study.
Study Design
Study Description
Connect with a study center
Peking Union Medical College Hospital
Beijing, Beijing 100730
ChinaActive - Recruiting

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