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NCT02267044 · ClinicalTrials.gov registry record · NA
Effective Pain Management of Interscalene Blocks During Shoulder Surgery
A NA study of Primary Osteoarthritis, Unspecified Shoulder, sponsored by TriHealth.
- Completed
- Registry status
- NA
- Development phase
- 76
- Enrollment target
- 1
- Study location
NCT02267044: Completed NA study of Primary Osteoarthritis, Unspecified Shoulder, sponsored by TriHealth.
NCT02267044 is a NA study of Primary Osteoarthritis, Unspecified Shoulder that has completed, run by TriHealth. The registered enrollment target is 76 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02267044, a NA study of Primary Osteoarthritis, Unspecified Shoulder, has completed, sponsored by TriHealth.
- COMPLETED
- Registry status
- NA
- Development phase
- 76 participants
- Enrollment target
- 1
- Study location
Study Summary
Shoulder replacement surgery is recognized as having the potential to cause a considerable amount of postoperative pain. Adequate management of pain after surgery is necessary not only to improve the patient's wellbeing but also to facilitate recovery. Several regional anesthesia techniques are available to combat postoperative pain in the shoulder replacement surgery patient, however, which method provides superior pain relief remains unknown. The purpose of this study is to examine the effectiveness of a continuous interscalene block versus a single shot interscalene block for postoperative pain relief in the shoulder replacement patient. Patients undergoing shoulder replacement surgery will experience more effective pain relief with a continuous interscalene block versus and single shot interscalene block.
Primary Outcome
Patients will be assessed for pain levels by visual analog scale while in the hospital per nursing protocol. Electronic Medical Record will be used to acquire pain scores.
Conditions Studied
Interventions
- DRUG Ropivacaine
Study Locations (1)
Ohio
- Good Samaritan Hospital - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 76 participants |
| Start Date | 2014-08 |
| Est. Completion | 2017-04 |
| Phase | NA |
What the finished NCT02267044 record still lists
NCT02267044 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 1 condition, with Primary Osteoarthritis, Unspecified Shoulder appearing as the primary indexed condition, and to 1 intervention - of which Ropivacaine is the first listed.
NCT02267044 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT02267044 about?
NCT02267044 is a clinical study titled "Effective Pain Management of Interscalene Blocks During Shoulder Surgery". Shoulder replacement surgery is recognized as having the potential to cause a considerable amount of postoperative pain. Adequate management of pain after surgery is necessary not only to improve the patient's wellbeing but also to facilitate recovery. Several regional anesthesia techniques are avai...
What is the current status of trial NCT02267044?
This trial is currently completed. It is a NA study. The enrollment target is 76 participants. The study started on 2014-08. Estimated completion is 2017-04.
What conditions does trial NCT02267044 study?
This clinical trial studies the following conditions: Primary Osteoarthritis, Unspecified Shoulder.
What interventions are being tested in trial NCT02267044?
The interventions under investigation include: Ropivacaine (DRUG).
Who is sponsoring clinical trial NCT02267044?
This trial is sponsored by TriHealth, which has 81 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02267044 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
How this trial's enrollment target compares
Where NCT02267044's enrollment target sits among peer trials
76 1062nd of 2000 higher than 932 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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.
Source ClinicalTrials.gov registry export · 2026-08-08
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