Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02697123 · ClinicalTrials.gov registry record
Prospective Assessment of the Deep Vein Thrombosis (DVT) in Hospitalized Obstetrics Patients
A clinical trial, sponsored by Baylor College of Medicine.
- Terminated
- Registry status
- 5
- Enrollment target
NCT02697123: Clinical Trial study, sponsored by Baylor College of Medicine.
NCT02697123 is a clinical trial that was terminated before completion, run by Baylor College of Medicine. The registered enrollment target is 5 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02697123 was terminated before completion, sponsored by Baylor College of Medicine.
- TERMINATED
- Registry status
- 5 participants
- Enrollment target
Study Summary
The purpose of the study is to prospectively assess the prevalence of venous thrombosis in women hospitalized for Cesarean Section, vaginal delivery or extended antepartum hospitalization by using Compression ultrasound of the entire proximal venous system of the lower limb veins.
Interventions
- OTHER antepartum and postpartum
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2016-02 |
| Est. Completion | 2019-08 |
Why NCT02697123 stopped before completion
NCT02697123 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 5 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which antepartum and postpartum is the first listed.
NCT02697123 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02697123 about?
NCT02697123 is a clinical study titled "Prospective Assessment of the Deep Vein Thrombosis (DVT) in Hospitalized Obstetrics Patients". The purpose of the study is to prospectively assess the prevalence of venous thrombosis in women hospitalized for Cesarean Section, vaginal delivery or extended antepartum hospitalization by using Compression ultrasound of the entire proximal venous system of the lower limb veins.
What is the current status of trial NCT02697123?
This trial is currently terminated. The enrollment target is 5 participants. The study started on 2016-02. Estimated completion is 2019-08.
What interventions are being tested in trial NCT02697123?
The interventions under investigation include: antepartum and postpartum (OTHER).
Who is sponsoring clinical trial NCT02697123?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
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