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NCT04109638 · ClinicalTrials.gov registry record · NA
Pulsed Electromagnetic Field (PEMF) Therapy for Post-operative Pain Following Orthopedic Surgery
A NA study of Pain, Postoperative and Knee Injuries, sponsored by Stanford University.
- Recruiting
- Registry status
- NA
- Development phase
- 76
- Enrollment target
- 1
- Study location
NCT04109638 is a NA study of Pain, Postoperative and Knee Injuries that is actively recruiting participants, run by Stanford University. The registered enrollment target is 76 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (72% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04109638, a NA study of Pain, Postoperative and Knee Injuries, is actively recruiting participants, sponsored by Stanford University.
- RECRUITING
- Registry status
- NA
- Development phase
- 76 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective of this study is to prospectively determine, at 10 days after orthopedic shoulder or knee surgery, if pulsed electromagnetic field (PEMF) therapy is beneficial in reducing patient-reported post-operative pain, as measured by visual analog scale (VAS). The amount of pain medication taken daily and the physical function outcome scores after surgery and PEMF treatment will also be measured.
Conditions Studied
Interventions
- DEVICE Endonovo SofPulse
Study Locations (1)
California
- Stanford University - Redwood City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 76 participants |
| Start Date | 2021-02-01 |
| Est. Completion | 2027-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04109638
The ClinicalTrials.gov registry entry for NCT04109638 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 76 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (72% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 1 intervention - of which Endonovo SofPulse is the first listed.
NCT04109638 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT04109638 about?
NCT04109638 is a clinical study titled "Pulsed Electromagnetic Field (PEMF) Therapy for Post-operative Pain Following Orthopedic Surgery". The primary objective of this study is to prospectively determine, at 10 days after orthopedic shoulder or knee surgery, if pulsed electromagnetic field (PEMF) therapy is beneficial in reducing patient-reported post-operative pain, as measured by visual analog scale (VAS). The amount of pain medicat...
What is the current status of trial NCT04109638?
This trial is currently recruiting. It is a NA study. The enrollment target is 76 participants. The study started on 2021-02-01. Estimated completion is 2027-02.
What conditions does trial NCT04109638 study?
This clinical trial studies the following conditions: Pain, Postoperative, Knee Injuries, Shoulder Injuries.
What interventions are being tested in trial NCT04109638?
The interventions under investigation include: Endonovo SofPulse (DEVICE).
Who is sponsoring clinical trial NCT04109638?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04109638 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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