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

NCT02618382 · ClinicalTrials.gov registry record · Phase 4

A Study on the Safety of Tranexamic Acid for the Chronic Subdural Hematoma Population

A Phase 4 study, sponsored by St. Joseph's Hospital and Medical Center, Phoenix.

Completed
Registry status
Phase 4
Development phase
32
Enrollment target

NCT02618382: Completed Phase 4 study, sponsored by St. Joseph's Hospital and Medical Center, Phoenix.

NCT02618382 is a Phase 4 study that has completed, run by St. Joseph's Hospital and Medical Center, Phoenix. The registered enrollment target is 32 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02618382, a Phase 4 study, has completed, sponsored by St. Joseph's Hospital and Medical Center, Phoenix.

COMPLETED
Registry status
Phase 4
Development phase
32 participants
Enrollment target

Study Summary

This is a single center single arm study of 50 patients to 1) determine the safety of tranexamic acid in the chronic subdural hematoma population following surgical drainage of chronic subdural hematomas and 2) determine if the use of oral tranexamic acid reduces the rate of ipsilateral recurrence following drainage of chronic subdural hematomas. This will be compared to historical controls. This study intends to be a prerequisite to a large nationally funded randomized control trial.

Primary Outcome

occurrence of stroke, myocardial infarction, deep vein thrombosis, and/or pulmonary embolism within 30 days

Interventions

  • DRUG Tranexamic Acid

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2015-11-01
Est. Completion 2018-06-12
Phase Phase 4

What the finished NCT02618382 record still lists

NCT02618382 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (94% lower).

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

NCT02618382 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02618382 about?

NCT02618382 is a clinical study titled "A Study on the Safety of Tranexamic Acid for the Chronic Subdural Hematoma Population". This is a single center single arm study of 50 patients to 1) determine the safety of tranexamic acid in the chronic subdural hematoma population following surgical drainage of chronic subdural hematomas and 2) determine if the use of oral tranexamic acid reduces the rate of ipsilateral recurrence f...

What is the current status of trial NCT02618382?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 32 participants. The study started on 2015-11-01. Estimated completion is 2018-06-12.

What interventions are being tested in trial NCT02618382?

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

Who is sponsoring clinical trial NCT02618382?

This trial is sponsored by St. Joseph's Hospital and Medical Center, Phoenix, which has 44 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02618382's enrollment target sits among peer trials

32 1534th of 2000 higher than 457 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

  • NCT02445781 · 32 participants · Early Phase 1

    Differing Levels of Hypoglycemia

  • NCT02792270 · 32 participants · NA

    Caloric Restriction In Sarcoma Patients Treated With Pre-Operative RT

  • NCT03068910 · 32 participants · Early Phase 1

    Hyperandrogenemia and Altered Day-night LH Pulse Patterns

  • NCT03208868 · 32 participants · NA

    Leucine Enriched Essential Amino Acid Mixture to Reverse Muscle Loss in Cirrhosis

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 NCT02618382, the US trial registry maintained by the National Library of Medicine. NCT02618382 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.