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NCT06118957 · ClinicalTrials.gov registry record · Phase 2

Low Molecular Weight Heparin or no Treatment Following Cesarean Delivery

A Phase 2 study of Thromboembolism, sponsored by University of Utah.

Completed
Registry status
Phase 2
Development phase
64
Enrollment target
1
Study location

NCT06118957 is a Phase 2 study of Thromboembolism that has completed, run by University of Utah. The registered enrollment target is 64 participants, below the 307-participant average among 8 other Thromboembolism trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06118957, a Phase 2 study of Thromboembolism, has completed, sponsored by University of Utah.

COMPLETED
Registry status
Phase 2
Development phase
64 participants
Enrollment target
1
Study location

Study Summary

The aim of this study is to evaluate the feasibility of randomizing individuals to low molecular weight heparin (enoxaparin) or no treatment following cesarean delivery. The investigators hypothesize that among eligible individuals, at least 35% will enroll, undergo randomization, and complete the allocated treatment group.

Conditions Studied

Interventions

  • DRUG Enoxaparin

Study Locations (1)

Utah

  • University of Utah - Salt Lake City

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2023-10-11
Est. Completion 2024-07-01
Phase Phase 2

Sponsor

University of Utah

818 total trials

What the Registry Record Tells You About NCT06118957

The ClinicalTrials.gov registry entry for NCT06118957 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 307-participant average among 8 other Thromboembolism trials with a reported enrollment target (79% lower). The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Thromboembolism appearing as the primary indexed condition, and to 1 intervention - of which Enoxaparin is the first listed.

NCT06118957 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.

Frequently Asked Questions

What is clinical trial NCT06118957 about?

NCT06118957 is a clinical study titled "Low Molecular Weight Heparin or no Treatment Following Cesarean Delivery". The aim of this study is to evaluate the feasibility of randomizing individuals to low molecular weight heparin (enoxaparin) or no treatment following cesarean delivery. The investigators hypothesize that among eligible individuals, at least 35% will enroll, undergo randomization, and complete the a...

What is the current status of trial NCT06118957?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 64 participants. The study started on 2023-10-11. Estimated completion is 2024-07-01.

What conditions does trial NCT06118957 study?

This clinical trial studies the following conditions: Thromboembolism.

What interventions are being tested in trial NCT06118957?

The interventions under investigation include: Enoxaparin (DRUG).

Who is sponsoring clinical trial NCT06118957?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06118957 being conducted?

This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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