Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02411396 · ClinicalTrials.gov registry record
Comparison of Patient Centered Outcomes for People With Sickle Cell Disease in the Acute Care Setting
A clinical trial, sponsored by Johns Hopkins University.
- Completed
- Registry status
- 483
- Enrollment target
NCT02411396: Completed study, sponsored by Johns Hopkins University.
NCT02411396 is a clinical trial that has completed, run by Johns Hopkins University. The registered enrollment target is 483 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02411396 has completed, sponsored by Johns Hopkins University.
- COMPLETED
- Registry status
- 483 participants
- Enrollment target
Study Summary
The Emergency Department has been the standard location where patients with Sickle Cell Disease (SCD) go to seek care for the treatment of acute painful events. Vaso- Occlusive Crisis (VOC) is the most common complication of SCD, The purpose of this study is to compare patient centered outcomes for patients being treated for an uncomplicated VOC in Infusion Centers (IC) and Emergency Departments (ED) in four locations around the United States.
Primary Outcome
Time is recorded from the time the patient arrives for pain treatment at either the ED or IC until the time the patient is dosed with pain medication administered parenterally. Guideline recommendations are that patients receive non-oral pain medication within 60 minutes of arrival.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 483 participants |
| Start Date | 2015-04 |
| Est. Completion | 2018-06 |
What the finished NCT02411396 record still lists
NCT02411396 is an observational study that tracks outcomes without assigning an intervention. The registered 483 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT02411396 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02411396 about?
NCT02411396 is a clinical study titled "Comparison of Patient Centered Outcomes for People With Sickle Cell Disease in the Acute Care Setting". The Emergency Department has been the standard location where patients with Sickle Cell Disease (SCD) go to seek care for the treatment of acute painful events. Vaso- Occlusive Crisis (VOC) is the most common complication of SCD, The purpose of this study is to compare patient centered outcomes for...
What is the current status of trial NCT02411396?
This trial is currently completed. The enrollment target is 483 participants. The study started on 2015-04. Estimated completion is 2018-06.
Who is sponsoring clinical trial NCT02411396?
This trial is sponsored by Johns Hopkins University, which has 1,448 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 enrollment target
- NCT02871726 · 483 participants · NA
Transrectal Ultrasound Robot-Assisted Prostate Biopsy
- NCT05421741 · 484 participants · Phase 4
Prophylactic Antibiotic Coated Nail to Prevent Infection: A Clinical Trial
- NCT04449458 · 482 participants · NA
The Positively Quit Trial for Smoking Cessation
- NCT07079631 · 482 participants · Phase 1
A Clinical Study to Test if an Investigational Treatment Called BNT314 When Used in Combination With Another Investigational Treatment BNT327 and Chemotherapy, is Beneficial and Safe for Patients With Advanced Colorectal Cancer
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