Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01888003 · ClinicalTrials.gov registry record · NA

The Benefits of a Preoperative Anemia Management Program

A NA study, sponsored by University of Alabama at Birmingham.

Terminated
Registry status
NA
Development phase
51
Enrollment target

NCT01888003: Clinical Trial NA study, sponsored by University of Alabama at Birmingham.

NCT01888003 is a NA study that was terminated before completion, run by University of Alabama at Birmingham. The registered enrollment target is 51 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01888003, a NA study, was terminated before completion, sponsored by University of Alabama at Birmingham.

TERMINATED
Registry status
NA
Development phase
51 participants
Enrollment target

Study 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

Primary Outcome

The number of subjects who had blood transfusions (at least 1) during surgery

Interventions

  • DRUG Iron sucrose
  • DRUG Epoetin Alfa
  • OTHER Blood Transfusion

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2013-04
Est. Completion 2015-01
Phase NA
University of Alabama at Birmingham

1,160 total trials

Why NCT01888003 stopped before completion

NCT01888003 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 3 interventions - of which Iron sucrose is the first listed.

NCT01888003 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01888003 about?

NCT01888003 is a clinical study titled "The Benefits of a Preoperative Anemia Management Program". 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 (...

What is the current status of trial NCT01888003?

This trial is currently terminated. It is a NA study. The enrollment target is 51 participants. The study started on 2013-04. Estimated completion is 2015-01.

What interventions are being tested in trial NCT01888003?

The interventions under investigation include: Iron sucrose (DRUG), Epoetin Alfa (DRUG), Blood Transfusion (OTHER).

Who is sponsoring clinical trial NCT01888003?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01888003's enrollment target sits among peer trials

51 1279th of 2000 higher than 722 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02701153 · 51 participants · NA

    Phase II Study of 5-Day Hypofractionated Preoperative Radiation Therapy for Soft Tissue Sarcomas: Expansion Cohort

  • NCT03663790 · 51 participants · NA

    Effects of Gait Retraining on Lower Extremity Biomechanics

  • NCT03874052 · 51 participants · Phase 1

    Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia

  • NCT04704661 · 51 participants · Phase 1

    Testing the Combination of Two Anti-cancer Drugs, DS-8201a and AZD6738, for The Treatment of Advanced Solid Tumors Expressing the HER2 Protein or Gene, The DASH Trial

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01888003, the US trial registry maintained by the National Library of Medicine. NCT01888003 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.