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

NCT00878826 · ClinicalTrials.gov registry record · Phase 2

Prophylactic Enoxaparin Dosing for Prevention of Venous Thromboembolism in Pregnancy.

A Phase 2 study, sponsored by Stanford University.

Completed
Registry status
Phase 2
Development phase
11
Enrollment target

NCT00878826: Completed Phase 2 study, sponsored by Stanford University.

NCT00878826 is a Phase 2 study that has completed, run by Stanford University. The registered enrollment target is 11 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT00878826, a Phase 2 study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
Phase 2
Development phase
11 participants
Enrollment target

Study Summary

Enoxaparin is a type of low molecular weight heparin (LMWH), or anticoagulant, used to prevent and treat blood clots. Formation of blood clots, or venous thromboemboli (VTE) in pregnancy can have dangerous and even life-threatening effects on the mother and fetus. Enoxaparin is the preferred medicine to prevent clotting in pregnant patients who are at risk for VTE, because it has been studied to be safe and effective in pregnancy without any harms to the fetus. Although this medication is routinely used and is recommended by several prominent medical groups, the optimal dosing for prevention of VTE is still unclear. The range of standardly prescribed dosing regimens of Enoxaparin includes 40mg daily and 1mg/kg daily, but these two dosing strategies have never been compared in a head to head fashion.

Primary Outcome

Goal peak anti-Xa level is 0.2 to 0.4 u/ml. We compared peak drug levels between different dosing arms.

Interventions

  • DRUG Enoxaparin

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2009-05
Est. Completion 2014-10
Phase Phase 2
Stanford University

1,744 total trials

What the finished NCT00878826 record still lists

NCT00878826 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

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

NCT00878826 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00878826 about?

NCT00878826 is a clinical study titled "Prophylactic Enoxaparin Dosing for Prevention of Venous Thromboembolism in Pregnancy.". Enoxaparin is a type of low molecular weight heparin (LMWH), or anticoagulant, used to prevent and treat blood clots. Formation of blood clots, or venous thromboemboli (VTE) in pregnancy can have dangerous and even life-threatening effects on the mother and fetus. Enoxaparin is the preferred medicin...

What is the current status of trial NCT00878826?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2009-05. Estimated completion is 2014-10.

What interventions are being tested in trial NCT00878826?

The interventions under investigation include: Enoxaparin (DRUG).

Who is sponsoring clinical trial NCT00878826?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00878826's enrollment target sits among peer trials

11 1967th of 2000 higher than 33 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

  • NCT03114462 · 11 participants · Phase 1

    Trial of Stereotactic HYpofractionateD RadioAblative (HYDRA) Treatment of Laryngeal Cancer

  • NCT06039709 · 11 participants · Phase 1

    Sonodynamic Therapy in Patients With Recurrent GBM

  • NCT06425380 · 11 participants · NA

    Pilot Open-Label Trial of Resistant Potato Starch in Patients With Cirrhosis and Overt Hepatic Encephalopathy

  • NCT06472661 · 11 participants · Early Phase 1

    FUSA With Intratumoral PolyICLC in Regionally Advanced Resectable Melanoma

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 NCT00878826, the US trial registry maintained by the National Library of Medicine. NCT00878826 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.