Platelet Rich Plasma (PRP) in Total Knee Replacement

ClinicalTrials.gov ID: NCT00826098

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Official title

Platelet Rich Plasma (PRP) in Total Knee Replacement: A Prospective, Randomized, Single-blind, Single-center Clinical Study to Evaluate the Effect of Platelet Rich Plasma (PRP) on Short-term Patient Outcomes Following Total Knee Replacement

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Clinical study to evaluate the effect of platelet rich plasma (PRP), a derivative of a patient's whole blood, on short-term patient outcomes following total knee replacement (TKR).

Study identification

NCT ID: NCT00826098
Recruitment status: Completed
Study type: Interventional
Phase: Phase 4
Lead sponsor: Exactech; Industry
Enrollment: 70 participants

Conditions and interventions

Conditions

Interventions

Platelet Rich Plasma Biological

Biological

Eligibility (public fields only)

Age range: Not listed
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Dec 2008 (Type not available)
Primary completion: Jun 2011 (Actual)
Completion: Feb 2013 (Actual)
Last update posted: Sep 1, 2022

2008 – 2013

United States locations

U.S. sites: 2
U.S. states: 2
U.S. cities: 2

Facility	City	State	ZIP	Site status
Center for Joint Replacement, St. Mary's Regional Medical Center	Lewiston	Maine	04240	—
Peninsula Orthopedic Associates	Salisbury	Maryland	21804	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00826098, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Sep 1, 2022 · Synced Nov 13, 2026