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NCT01680549 · ClinicalTrials.gov registry record · Phase 4
Pain Control With Total Knee Replacement
A Phase 4 study of Postoperative Pain, sponsored by Texas Tech University Health Sciences Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT01680549: Completed Phase 4 study of Postoperative Pain, sponsored by Texas Tech University Health Sciences Center.
NCT01680549 is a Phase 4 study of Postoperative Pain that has completed, run by Texas Tech University Health Sciences Center. The registered enrollment target is 50 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01680549, a Phase 4 study of Postoperative Pain, has completed, sponsored by Texas Tech University Health Sciences Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this project is to study the effects of gabapentin on pain control in the perioperative and post-operative period of total knee arthroplasty.
Primary Outcome
Patient's pain assessed by the Visual Analog Scale (VAS - Units on a scale) on postoperative days 0, 1 and 2. Scale range: 0-100 Higher Values = More Pain
Conditions Studied
Interventions
- DRUG Gabapentin
Study Locations (1)
Texas
- TTUHSC Orthopaedic Surgery MS 9436 - Lubbock
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2012-09 |
| Est. Completion | 2016-02 |
| Phase | Phase 4 |
What the finished NCT01680549 record still lists
NCT01680549 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (78% lower).
The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 1 intervention - of which Gabapentin is the first listed.
NCT01680549 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT01680549 about?
NCT01680549 is a clinical study titled "Pain Control With Total Knee Replacement". The purpose of this project is to study the effects of gabapentin on pain control in the perioperative and post-operative period of total knee arthroplasty.
What is the current status of trial NCT01680549?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2012-09. Estimated completion is 2016-02.
What conditions does trial NCT01680549 study?
This clinical trial studies the following conditions: Postoperative Pain.
What interventions are being tested in trial NCT01680549?
The interventions under investigation include: Gabapentin (DRUG).
Who is sponsoring clinical trial NCT01680549?
This trial is sponsored by Texas Tech University Health Sciences Center, which has 76 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01680549 being conducted?
This trial has 1 study location across Texas. 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 NCT01680549's enrollment target sits among peer trials
50 102nd of 120 higher than 18 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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