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NCT02313675 · ClinicalTrials.gov registry record · Phase 4
Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol for Carpal Tunnel and Distal Radius Fracture Surgeries
A Phase 4 study of Postoperative Pain and Distal Radius Fracture, sponsored by John Fowler.
- Completed
- Registry status
- Phase 4
- Development phase
- 44
- Enrollment target
- 1
- Study location
NCT02313675 is a Phase 4 study of Postoperative Pain and Distal Radius Fracture that has completed, run by John Fowler. The registered enrollment target is 44 participants, below the 231-participant average among 63 other Postoperative Pain trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02313675, a Phase 4 study of Postoperative Pain and Distal Radius Fracture, has completed, sponsored by John Fowler.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 44 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the efficacy of intra-operative administration of IV tylenol and/or IV toradol in minimizing post-operative pain for carpal tunnel patients and distal radius fracture patients.
Conditions Studied
Interventions
- DRUG Acetaminophen
- DRUG Saline
- DRUG Ketorolac Tromethamine
Study Locations (1)
Pennsylvania
- Kaufmann Building - Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2015-05 |
| Est. Completion | 2017-05-01 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02313675
The ClinicalTrials.gov registry entry for NCT02313675 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 231-participant average among 63 other Postoperative Pain trials with a reported enrollment target (81% lower). The listed sponsor is John Fowler, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 3 interventions - of which Acetaminophen is the first listed.
NCT02313675 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT02313675 about?
NCT02313675 is a clinical study titled "Pain Outcomes of Intra-operative IV Tylenol and/or IV Toradol for Carpal Tunnel and Distal Radius Fracture Surgeries". The purpose of this study is to determine the efficacy of intra-operative administration of IV tylenol and/or IV toradol in minimizing post-operative pain for carpal tunnel patients and distal radius fracture patients.
What is the current status of trial NCT02313675?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 44 participants. The study started on 2015-05. Estimated completion is 2017-05-01.
What conditions does trial NCT02313675 study?
This clinical trial studies the following conditions: Postoperative Pain, Distal Radius Fracture, Carpal Tunnel Release.
What interventions are being tested in trial NCT02313675?
The interventions under investigation include: Acetaminophen (DRUG), Saline (DRUG), Ketorolac Tromethamine (DRUG).
Who is sponsoring clinical trial NCT02313675?
This trial is sponsored by John Fowler, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02313675 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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