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NCT02053363 · ClinicalTrials.gov registry record · Phase 2

Tranexamic Acid Dosing in Adult Spinal Deformity Surgery

A Phase 2 study, sponsored by Washington University School of Medicine.

Completed
Registry status
Phase 2
Development phase
64
Enrollment target

NCT02053363: Completed Phase 2 study, sponsored by Washington University School of Medicine.

NCT02053363 is a Phase 2 study that has completed, run by Washington University School of Medicine. The registered enrollment target is 64 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (52% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02053363, a Phase 2 study, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
Phase 2
Development phase
64 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate two dosing protocols for tranexamic acid (TXA), an anti-fibrinolytic used to decrease blood loss in adult patients undergoing complex, reconstructive spinal fusion surgeries.

Primary Outcome

To compare the estimated blood loss in patients undergoing complex, reconstructive, spinal fusion surgeries receiving one of two dosing protocols for the anti-fibrinolytic, TXA. Estimated blood loss was calculated by suction canister volume minus intraoperative irrigation fluid plus blood content in sponges as estimated by weight for all cases.

Interventions

  • DRUG Tranexamic Acid (Cyklokapron)

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2014-03
Est. Completion 2020-06-26
Phase Phase 2

What the finished NCT02053363 record still lists

NCT02053363 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (52% lower).

The record links to 0 conditions, and to 1 intervention - of which Tranexamic Acid (Cyklokapron) is the first listed.

NCT02053363 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02053363 about?

NCT02053363 is a clinical study titled "Tranexamic Acid Dosing in Adult Spinal Deformity Surgery". The purpose of this study is to evaluate two dosing protocols for tranexamic acid (TXA), an anti-fibrinolytic used to decrease blood loss in adult patients undergoing complex, reconstructive spinal fusion surgeries.

What is the current status of trial NCT02053363?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 64 participants. The study started on 2014-03. Estimated completion is 2020-06-26.

What interventions are being tested in trial NCT02053363?

The interventions under investigation include: Tranexamic Acid (Cyklokapron) (DRUG).

Who is sponsoring clinical trial NCT02053363?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02053363's enrollment target sits among peer trials

64 996th of 2000 higher than 992 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT02053363, the US trial registry maintained by the National Library of Medicine. NCT02053363 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.