Clinical Trials Logo

Clinical Trial Summary

The goal of this study is to gain further insight into the comparative effectiveness of treating patients, who are found to be anemic before their elective surgery, with a series of weekly subcutaneous doses of a drug given before surgery, which stimulates the natural production of red blood cells (a so-called erythropoietic stimulating agent [ESA]) along with intravenous iron, in reducing the need for blood transfusions (donated by someone other than the patient) during and after adult total hip arthroplasty (hip replacement surgery). The effects of a Preoperative Anemia Management Program (PAMP) on the patient's quality of recovery, health-related quality of life, fatigue, and rehabilitation pattern after surgery will also be examined. A cost-effectiveness analysis will be performed to compare the cost of these commercially available, FDA-approved medications versus the cost of transfused blood


Clinical Trial Description

Patient blood management (PBM) involves the timely and conscientious use of the current best evidence in making medical and surgical decisions about the care of patients to maintain red blood cell levels, optimize blood clotting, and minimize blood loss, in an effort to improve patient outcome. PBM focuses on the treatment of the individual patient and comprises transfusion therapy and drug therapy. PBM is based on three points: (1) optimization of the (preoperative) red blood cell volume, (2) reduction of diagnostic, therapeutic, or intraoperative blood loss, and (3) increasing individual tolerance towards anemia and accurate blood transfusion triggers. PBM primarily identifies patients at risk for transfusion and provides a management plan aimed at reducing or eliminating anemia and the need for blood transfusion donated from someone other than the patient (allogeneic transfusion), thus reducing the risks, blood bank inventory pressures, and the escalating costs associated with transfusion. The implementation of a formal UAB Preoperative Anemia Management Program (PAMP) may help achieve consistent PBM.

Efforts will be made to coordinate patients' scheduled surgery date and their initial evaluation in the UAB Highlands Hospital Preoperative Assessment, Consultation, and Treatment (HPACT) Clinic, so that their first PACT Clinic visit occurs approximately 14 days prior to the planned total hip replacement or total knee replacement ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01888003
Study type Interventional
Source University of Alabama at Birmingham
Contact
Status Terminated
Phase N/A
Start date April 2013
Completion date January 2015

See also
  Status Clinical Trial Phase
Active, not recruiting NCT03516734 - Iron-fortified Lentils to Improve Iron (Fe) Status in Bangladesh N/A
Completed NCT02570854 - A Two-part Single- and Repeat-dose Study of CSJ137 in Anemic Chronic Hemodialysis Patients Phase 1
Completed NCT02887963 - Epidemiological Study of Iron Deficiency and Iron Deficiency Anemia in Chinese Pregnant Women N/A
Completed NCT00534144 - Comparison Between Effects of Two Iron Preparations on Protein in the Urine Phase 1
Completed NCT00224081 - DRIVE Trial (Dialysis Patients' Response to Intravenous [IV] Iron With Elevated Ferritin) Phase 4
Recruiting NCT02999217 - Intravenous Iron for Correction of Anaemia After Colorectal Surgery Phase 4
Recruiting NCT04351607 - Preoperative Supplementation of Sucrosomal Iron as Hematopoietic Support. N/A
Completed NCT04163406 - The Effect of Human Milk Oligosaccharides and Galacto-oligosaccharides on Iron Absorption in Kenyan Infants N/A
Completed NCT02365103 - Tea Consumption and Iron Bioavailability in Women Using a Stable Isotope N/A
Completed NCT00536666 - A Study of Iron Oligosaccharide in Chronic Kidney Disease Patients Phase 3
Completed NCT02310607 - Non-invasive Optical Detection of Iron Deficiency N/A
Completed NCT01755455 - Does a Daily Iron Tablet Improve Anemia in Cystic Fibrosis N/A
Terminated NCT00929409 - Controlled Randomised Trial of Ferric Carboxymaltose and Oral Iron to Treat Postpartum Anemia Phase 2/Phase 3
Completed NCT00354692 - Effect of Two Iron Preparations on Protein in the Urine Phase 4
Recruiting NCT05628896 - Efficacy of a Preoperative Anaemia Clinic in Patients Undergoing Elective Abdominal Surgery
Completed NCT02892461 - Effect of Umbilical Cord Milking on Iron Related Health Outcomes for Cesarean-Delivered Infants N/A
Completed NCT02905539 - A Study Comparing the Iron Substitution With the Medicinal Products Ferinject or Monofer Phase 4
Not yet recruiting NCT01840384 - Efficacy Study of Multiple Micro Nutrients Supplementation N/A
Recruiting NCT00125996 - Effect of Intravenous Ferrous Sucrose on Exercise Capacity in Chronic Heart Failure Phase 1/Phase 2
Not yet recruiting NCT04975074 - Iron Deficiency Anemia in Twin Pregnancies Phase 4