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NCT01333969 · ClinicalTrials.gov registry record · NA
Ischemic Preconditioning in Total Knee Arthroplasty
A NA study, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT01333969 is a NA study that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 60 participants.
The verdict
NCT01333969, a NA study, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
The application of a tourniquet for 5 minutes and subsequent reperfusion before actual inflation of the tourniquet for total knee arthroplasty (ischemic preconditioning) decreases the level of local inflammation and therefore postoperative pain in response to reperfusion of the ischemic extremity.
Interventions
- PROCEDURE Ischemic Preconditioning
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2011-04 |
| Est. Completion | 2012-04 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01333969
The ClinicalTrials.gov registry entry for NCT01333969 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hospital for Special Surgery, New York, which has 194 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Ischemic Preconditioning is the first listed.
NCT01333969 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01333969 about?
NCT01333969 is a clinical study titled "Ischemic Preconditioning in Total Knee Arthroplasty". The application of a tourniquet for 5 minutes and subsequent reperfusion before actual inflation of the tourniquet for total knee arthroplasty (ischemic preconditioning) decreases the level of local inflammation and therefore postoperative pain in response to reperfusion of the ischemic extremity.
What is the current status of trial NCT01333969?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2011-04. Estimated completion is 2012-04.
What interventions are being tested in trial NCT01333969?
The interventions under investigation include: Ischemic Preconditioning (PROCEDURE).
Who is sponsoring clinical trial NCT01333969?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
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