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

NCT01536496 · ClinicalTrials.gov registry record · NA

Comparison of Rapid Thrombelastography and Conventional Coagulation Testing for Haemostatic Resuscitation in Trauma

A NA study, sponsored by Denver Health and Hospital Authority.

Completed
Registry status
NA
Development phase
114
Enrollment target

NCT01536496: Completed NA study, sponsored by Denver Health and Hospital Authority.

NCT01536496 is a NA study that has completed, run by Denver Health and Hospital Authority. The registered enrollment target is 114 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01536496, a NA study, has completed, sponsored by Denver Health and Hospital Authority.

COMPLETED
Registry status
NA
Development phase
114 participants
Enrollment target

Study Summary

The purpose of this study is to compare rapid thrombelastography (r-TEG) with conventional coagulation testing for diagnosing and treating coagulation abnormalities in severely injured patients who are likely to require transfusion therapy.

Interventions

  • BIOLOGICAL Blood product transfusion based on conventional coagulation tests.
  • BIOLOGICAL Blood product transfusion based on rapid thrombelastography (r-TEG) results.

Trial Details

FieldValue
Enrollment Target 114 participants
Start Date 2010-09
Est. Completion 2014-07
Phase NA

What the finished NCT01536496 record still lists

NCT01536496 is an interventional study that assigns participants to a tested intervention. The registered 114 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which Blood product transfusion based on conventional coagulation tests. is the first listed.

NCT01536496 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01536496 about?

NCT01536496 is a clinical study titled "Comparison of Rapid Thrombelastography and Conventional Coagulation Testing for Haemostatic Resuscitation in Trauma". The purpose of this study is to compare rapid thrombelastography (r-TEG) with conventional coagulation testing for diagnosing and treating coagulation abnormalities in severely injured patients who are likely to require transfusion therapy.

What is the current status of trial NCT01536496?

This trial is currently completed. It is a NA study. The enrollment target is 114 participants. The study started on 2010-09. Estimated completion is 2014-07.

What interventions are being tested in trial NCT01536496?

The interventions under investigation include: Blood product transfusion based on conventional coagulation tests. (BIOLOGICAL), Blood product transfusion based on rapid thrombelastography (r-TEG) results. (BIOLOGICAL).

Who is sponsoring clinical trial NCT01536496?

This trial is sponsored by Denver Health and Hospital Authority, which has 73 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01536496's enrollment target sits among peer trials

114 811th of 2000 higher than 1,188 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

  • NCT04522791 · 114 participants · Phase 2

    Breathing, Relaxation, Attention Training, & Health in Older Adults (BREATHE)

  • NCT04875052 · 114 participants · NA

    Vibration and Post-traumatic Osteoarthritis Risk Following ACL Injury

  • NCT05100342 · 114 participants

    Prospective Validation of a Points Score System Predicting 30-day Survival

  • NCT05224089 · 114 participants · Phase 4

    Bilateral TAP and RS Blocks Using Liposomal Bupivacaine/Bupivacaine vs. Regular Bupivacaine in Laparoscopic Colectomy

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 NCT01536496, the US trial registry maintained by the National Library of Medicine. NCT01536496 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.