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NCT02620748 · ClinicalTrials.gov registry record · Phase 1
Use of Intravenous Tranexamic Acid During Myomectomy
A Phase 1 study of Fibroids and Hemorrhage/Blood Loss During Myomectomies, sponsored by George Washington University.
- Completed
- Registry status
- Phase 1
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT02620748 is a Phase 1 study of Fibroids and Hemorrhage/Blood Loss During Myomectomies that has completed, run by George Washington University. The registered enrollment target is 60 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02620748, a Phase 1 study of Fibroids and Hemorrhage/Blood Loss During Myomectomies, has completed, sponsored by George Washington University.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the effect of the early administration of intravenous (IV) Tranexamic acid (TA) on perioperative bleeding (as defined by measured intraoperative estimated blood loss (EBL), change in pre and post-operative hemoglobin (Hb), and frequency of blood transfusions) in women undergoing a myomectomy.
Conditions Studied
Interventions
- DRUG Tranexamic Acid
- OTHER Saline Solution
Study Locations (1)
District of Columbia
- Medical Faculty Associates - Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2015-03 |
| Est. Completion | 2018-02-22 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02620748
The ClinicalTrials.gov registry entry for NCT02620748 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is George Washington University, which has 133 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Fibroids appearing as the primary indexed condition, and to 2 interventions - of which Tranexamic Acid is the first listed.
NCT02620748 reports 1 study location spanning 1 distinct geographic area - top geographies include District of Columbia.
Frequently Asked Questions
What is clinical trial NCT02620748 about?
NCT02620748 is a clinical study titled "Use of Intravenous Tranexamic Acid During Myomectomy". The purpose of this study is to determine the effect of the early administration of intravenous (IV) Tranexamic acid (TA) on perioperative bleeding (as defined by measured intraoperative estimated blood loss (EBL), change in pre and post-operative hemoglobin (Hb), and frequency of blood transfusions...
What is the current status of trial NCT02620748?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2015-03. Estimated completion is 2018-02-22.
What conditions does trial NCT02620748 study?
This clinical trial studies the following conditions: Fibroids, Hemorrhage/Blood Loss During Myomectomies.
What interventions are being tested in trial NCT02620748?
The interventions under investigation include: Tranexamic Acid (DRUG), Saline Solution (OTHER).
Who is sponsoring clinical trial NCT02620748?
This trial is sponsored by George Washington University, which has 133 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02620748 being conducted?
This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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