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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: Completed Phase 4 study of Postoperative Pain and Distal Radius Fracture, sponsored by John Fowler.
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 120 other Postoperative Pain trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
This is an ordinal pain scale. The patient picks a number from 0-10 scale every 4 hours for 7 days post-operatively. 0 is no pain, 10 is the worst pain imaginable. Lower scores would be preferable to higher scores.
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 |
What the finished NCT02313675 record still lists
NCT02313675 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (81% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Postoperative Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02313675's enrollment target sits among peer trials
44 106th of 120 higher than 15 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative 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.
Source ClinicalTrials.gov registry export · 2026-08-08
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