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NCT01599403 · ClinicalTrials.gov registry record · NA
Thoracic Blocks Versus Thoracic Epidural and Patient Controlled Anesthesia in Traumatic Rib Fracture Patients
A NA study of Traumatic Rib Fracture, sponsored by Brigham and Women's Hospital.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT01599403 is a NA study of Traumatic Rib Fracture that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 50 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01599403, a NA study of Traumatic Rib Fracture, has completed, sponsored by Brigham and Women's Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective of this study is to investigate whether continuous PVB is equal in efficacy to epidural anesthesia in terms of analgesia in patients with INR lower than 1.2, or is continuous ICNB equal in efficacy to PCA in terms of analgesia, if patients have INRs equal to or greater than 1.2.
Conditions Studied
Interventions
- PROCEDURE Paravertebral Block
- PROCEDURE Intercostal Nerve Block
- PROCEDURE Epidural Block
Study Locations (1)
Massachusetts
- Brigham and Women's Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2012-04 |
| Est. Completion | 2017-02-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01599403
The ClinicalTrials.gov registry entry for NCT01599403 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Brigham and Women's Hospital, which has 937 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Traumatic Rib Fracture appearing as the primary indexed condition, and to 3 interventions - of which Paravertebral Block is the first listed.
NCT01599403 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT01599403 about?
NCT01599403 is a clinical study titled "Thoracic Blocks Versus Thoracic Epidural and Patient Controlled Anesthesia in Traumatic Rib Fracture Patients". The primary objective of this study is to investigate whether continuous PVB is equal in efficacy to epidural anesthesia in terms of analgesia in patients with INR lower than 1.2, or is continuous ICNB equal in efficacy to PCA in terms of analgesia, if patients have INRs equal to or greater than 1.2...
What is the current status of trial NCT01599403?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2012-04. Estimated completion is 2017-02-01.
What conditions does trial NCT01599403 study?
This clinical trial studies the following conditions: Traumatic Rib Fracture.
What interventions are being tested in trial NCT01599403?
The interventions under investigation include: Paravertebral Block (PROCEDURE), Intercostal Nerve Block (PROCEDURE), Epidural Block (PROCEDURE).
Who is sponsoring clinical trial NCT01599403?
This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01599403 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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