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

NCT04475497 · ClinicalTrials.gov registry record · NA

Role of Blood Management in Perioperative Outcomes

A NA study, sponsored by The Cleveland Clinic.

Terminated
Registry status
NA
Development phase
18
Enrollment target

NCT04475497: Clinical Trial NA study, sponsored by The Cleveland Clinic.

NCT04475497 is a NA study that was terminated before completion, run by The Cleveland Clinic. The registered enrollment target is 18 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04475497, a NA study, was terminated before completion, sponsored by The Cleveland Clinic.

TERMINATED
Registry status
NA
Development phase
18 participants
Enrollment target

Study Summary

There is currently limited information regarding the role of blood management in the benign gynecologic population and specifically, in patients who are scheduled to undergo surgery for fibroids and/or abnormal uterine bleeding. A thorough search through PubMed and clinicaltrials.gov did not reveal any studies on this issue. In 2019 at CCF only 2% of gyn patients at Main Campus were referred to blood management, but 12.6% of the main campus gyn population had a Hb of \<10.0 g/dL. The overall goal of this study is to evaluate the role of preoperative blood management in optimizing surgical outcomes by reducing the co-morbidities associated with postoperative blood transfusion.

Primary Outcome

Preoperative hemoglobin minus postoperative hemoglobin

Interventions

  • OTHER Usual care
  • OTHER Blood management

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2020-07-24
Est. Completion 2023-05-18
Phase NA
The Cleveland Clinic

688 total trials

Why NCT04475497 stopped before completion

NCT04475497 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Usual care is the first listed.

NCT04475497 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04475497 about?

NCT04475497 is a clinical study titled "Role of Blood Management in Perioperative Outcomes". There is currently limited information regarding the role of blood management in the benign gynecologic population and specifically, in patients who are scheduled to undergo surgery for fibroids and/or abnormal uterine bleeding. A thorough search through PubMed and clinicaltrials.gov did not reveal ...

What is the current status of trial NCT04475497?

This trial is currently terminated. It is a NA study. The enrollment target is 18 participants. The study started on 2020-07-24. Estimated completion is 2023-05-18.

What interventions are being tested in trial NCT04475497?

The interventions under investigation include: Usual care (OTHER), Blood management (OTHER).

Who is sponsoring clinical trial NCT04475497?

This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04475497's enrollment target sits among peer trials

18 1863rd of 2000 higher than 130 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

  • NCT01245179 · 18 participants · Phase 1

    Study of Panobinostat (LBH589) in Patients With Sickle Cell Disease

  • NCT01999361 · 18 participants · NA

    Prevention of de Novo Allosensitization in Islet Transplant Recipients Following Complete Graft Loss

  • NCT02359825 · 18 participants · Phase 1

    Nerve Repair Using Hydrophilic Polymers to Promote Immediate Fusion of Severed Axons and Swift Return of Function

  • NCT02870244 · 18 participants · Phase 1

    Adoptive T Cell Immunotherapy for Advanced Melanoma Using Engineered Lymphocytes

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04475497, the US trial registry maintained by the National Library of Medicine. NCT04475497 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.