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NCT02769676 · ClinicalTrials.gov registry record · NA
A Comparison of Short Interval vs. Routine Postpartum Visit on Contraceptive Initiation
A NA study of Contraception, sponsored by Washington University School of Medicine.
- Completed
- Registry status
- NA
- Development phase
- 200
- Enrollment target
- 1
- Study location
NCT02769676 is a NA study of Contraception that has completed, run by Washington University School of Medicine. The registered enrollment target is 200 participants, below the 452-participant average among 72 other Contraception trials with a reported enrollment target (56% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02769676, a NA study of Contraception, has completed, sponsored by Washington University School of Medicine.
- COMPLETED
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
- 1
- Study location
Study Summary
The current postpartum care model of a single visit 4-6 weeks after delivery does not optimally address contraceptive needs. By this visit, many women have resumed sexual activity, potentially putting them at risk for unintended and rapid repeat pregnancy. In addition, many women with pregnancy-related Medicaid lose insurance coverage at this time, making it difficult to obtain long-acting reversible contraception (LARC) if desired. Therefore, an earlier postpartum visit may remove barriers to improve access to LARC thereby, reducing unintended and rapid repeat pregnancy. Our primary objective is to determine whether an additional 3-week postpartum visit, compared to usual postpartum care, will affect the initiation of LARC by 6 weeks postpartum.
Conditions Studied
Interventions
- OTHER usual care
- OTHER 3-week visit
Study Locations (1)
Missouri
- Washington University in St Louis - St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2016-05 |
| Est. Completion | 2018-05 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02769676
The ClinicalTrials.gov registry entry for NCT02769676 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 452-participant average among 72 other Contraception trials with a reported enrollment target (56% lower). The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Contraception appearing as the primary indexed condition, and to 2 interventions - of which usual care is the first listed.
NCT02769676 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.
Frequently Asked Questions
What is clinical trial NCT02769676 about?
NCT02769676 is a clinical study titled "A Comparison of Short Interval vs. Routine Postpartum Visit on Contraceptive Initiation". The current postpartum care model of a single visit 4-6 weeks after delivery does not optimally address contraceptive needs. By this visit, many women have resumed sexual activity, potentially putting them at risk for unintended and rapid repeat pregnancy. In addition, many women with pregnancy-rela...
What is the current status of trial NCT02769676?
This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2016-05. Estimated completion is 2018-05.
What conditions does trial NCT02769676 study?
This clinical trial studies the following conditions: Contraception.
What interventions are being tested in trial NCT02769676?
The interventions under investigation include: usual care (OTHER), 3-week visit (OTHER).
Who is sponsoring clinical trial NCT02769676?
This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02769676 being conducted?
This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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