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NCT02666118 · ClinicalTrials.gov registry record · NA
Efficacy of Nerve Blockade Performed Prior to Surgical Intervention Versus Following Surgical Intervention
A NA study of Pain and Shoulder Injury, sponsored by Children's Hospital Medical Center, Cincinnati.
- Active
- Registry status
- NA
- Development phase
- 79
- Enrollment target
- 1
- Study location
NCT02666118: Active NA study of Pain and Shoulder Injury, sponsored by Children's Hospital Medical Center, Cincinnati.
NCT02666118 is a NA study of Pain and Shoulder Injury that is active but no longer recruiting, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 79 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02666118, a NA study of Pain and Shoulder Injury, is active but no longer recruiting, sponsored by Children's Hospital Medical Center, Cincinnati.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 79 participants
- Enrollment target
- 1
- Study location
Study Summary
Nerve blocks, or pain medication injected next to the nerve while patients are asleep, are commonly used for pain management after shoulder surgery and are considered highly effective in decreasing post-operative pain. There are several different ways to give a nerve block. All are effective and safe. The purpose of this research is to determine if one of the available ways to give a nerve block is more effective than the others.
Conditions Studied
Interventions
- PROCEDURE Preemptive Interscalene Block - Single Shot
- PROCEDURE Postoperative Interscalene Block- Single Shot
- PROCEDURE Preemptive Interscalene Block - Catheter
- PROCEDURE Postoperative Interscalene Block - Catheter
Study Locations (1)
Ohio
- Cincinnati Children's Hospital Medical Center - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 79 participants |
| Start Date | 2013-02 |
| Est. Completion | 2025-03-31 |
| Phase | NA |
What the registry record for NCT02666118 still lists
NCT02666118 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 79 participants, a relatively small participant target, below the 304-participant average among 374 other Pain trials with a reported enrollment target (74% lower).
The record links to 2 conditions, with Pain appearing as the primary indexed condition, and to 4 interventions - of which Preemptive Interscalene Block - Single Shot is the first listed.
NCT02666118 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT02666118 about?
NCT02666118 is a clinical study titled "Efficacy of Nerve Blockade Performed Prior to Surgical Intervention Versus Following Surgical Intervention". Nerve blocks, or pain medication injected next to the nerve while patients are asleep, are commonly used for pain management after shoulder surgery and are considered highly effective in decreasing post-operative pain. There are several different ways to give a nerve block. All are effective and saf...
What is the current status of trial NCT02666118?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 79 participants. The study started on 2013-02. Estimated completion is 2025-03-31.
What conditions does trial NCT02666118 study?
This clinical trial studies the following conditions: Pain, Shoulder Injury.
What interventions are being tested in trial NCT02666118?
The interventions under investigation include: Preemptive Interscalene Block - Single Shot (PROCEDURE), Postoperative Interscalene Block- Single Shot (PROCEDURE), Preemptive Interscalene Block - Catheter (PROCEDURE), Postoperative Interscalene Block - Catheter (PROCEDURE).
Who is sponsoring clinical trial NCT02666118?
This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02666118 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT02666118's enrollment target sits among peer trials
79 205th of 374 higher than 170 of 374 other Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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