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NCT02690077 · ClinicalTrials.gov registry record · NA
Family-Centered Cesarean Delivery
A NA study of Patient Satisfaction and Earlier Family Bond Initiation, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 149
- Enrollment target
- 2
- Study locations
NCT02690077 is a NA study of Patient Satisfaction and Earlier Family Bond Initiation that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 149 participants, below the 460-participant average among 20 other Patient Satisfaction trials with a reported enrollment target (68% lower). The trial reports 2 study locations across 1 state.
The verdict
NCT02690077, a NA study of Patient Satisfaction and Earlier Family Bond Initiation, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 149 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this study is to determine if patient birthing experiences differ between the family-centered and traditional cesarean methods. We hypothesize that the family-centered cesarean method will lead to more unique and personalized cesarean birthing experiences without increasing the risks of adverse neonatal and maternal outcomes from those documented with the traditional cesarean.
Conditions Studied
Interventions
- PROCEDURE Family-Centered Cesarean
- PROCEDURE Traditional Cesarean
Study Locations (2)
Wisconsin
- Aurora BayCare Medical Center - Green Bay
- Aurora Sinai Medical Center - Milwaukee
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 149 participants |
| Start Date | 2016-06-01 |
| Est. Completion | 2021-10-29 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02690077
The ClinicalTrials.gov registry entry for NCT02690077 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 149 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 460-participant average among 20 other Patient Satisfaction trials with a reported enrollment target (68% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Patient Satisfaction appearing as the primary indexed condition, and to 2 interventions - of which Family-Centered Cesarean is the first listed.
NCT02690077 reports 2 study locations spanning 1 distinct geographic area - top geographies include Wisconsin.
Frequently Asked Questions
What is clinical trial NCT02690077 about?
NCT02690077 is a clinical study titled "Family-Centered Cesarean Delivery". The purpose of this study is to determine if patient birthing experiences differ between the family-centered and traditional cesarean methods. We hypothesize that the family-centered cesarean method will lead to more unique and personalized cesarean birthing experiences without increasing the risks ...
What is the current status of trial NCT02690077?
This trial is currently completed. It is a NA study. The enrollment target is 149 participants. The study started on 2016-06-01. Estimated completion is 2021-10-29.
What conditions does trial NCT02690077 study?
This clinical trial studies the following conditions: Patient Satisfaction, Earlier Family Bond Initiation, Maternal and Neonatal Outcomes.
What interventions are being tested in trial NCT02690077?
The interventions under investigation include: Family-Centered Cesarean (PROCEDURE), Traditional Cesarean (PROCEDURE).
Who is sponsoring clinical trial NCT02690077?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02690077 being conducted?
This trial has 2 study locations across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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