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COMPLETED NA

Family-Centered Cesarean Delivery

NCT02690077 · View on ClinicalTrials.gov ↗

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.

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

FieldValue
Enrollment Target 149 participants
Start Date 2016-06-01
Est. Completion 2021-10-29
Phase NA

Sponsor

Wake Forest University Health Sciences

1,061 total trials

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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. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 149 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,061 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02690077 reports 2 study locations spanning 1 distinct geographic area — top geographies include Wisconsin. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02690077?

The interventions under investigation include: Family-Centered Cesarean (PROCEDURE), Traditional Cesarean (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02690077?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,061 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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