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COMPLETED Phase 1

Use of Intravenous Tranexamic Acid During Myomectomy

NCT02620748 · View on ClinicalTrials.gov ↗

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.

Interventions

  • DRUG Tranexamic Acid
  • OTHER Saline Solution

Study Locations (1)

District of Columbia

  • Medical Faculty Associates — Washington D.C.

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2015-03
Est. Completion 2018-02-22
Phase Phase 1

Sponsor

George Washington University

134 total trials

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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. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. 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 134 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02620748 reports 1 study location spanning 1 distinct geographic area — top geographies include District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02620748?

The interventions under investigation include: Tranexamic Acid (DRUG), Saline Solution (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02620748?

This trial is sponsored by George Washington University, which has 134 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial