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ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

A Study to Investigate the Treatment Effect of Subcutaneous Injections of Pentosan Polysulfate Sodium Compared With Placebo in Adult Participants With Knee Osteoarthritis Pain.

ClinicalTrials.gov ID: NCT06917404

Public ClinicalTrials.gov record NCT06917404. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 8, 2026, 6:02 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomised, Double-Blind, Placebo-Controlled Multi-Centre Study to Evaluate the Treatment Effect of Pentosan Polysulfate Sodium Compared to Placebo in Participants With Knee Osteoarthritis Pain

Brief summary

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

The purpose of this study is to measure the change in pain and function with subcutaneous injections of pentosan polysulfate sodium (PPS) compared with subcutaneous injections of placebo in participants with knee OA pain. Study details include: * The study duration will be up to 64 weeks. * The treatment duration will be 6 weeks. * The visit frequency will be twice weekly during treatment. * The visit/contact frequency will be every 4-6 weeks during the 52-week Follow-up period. * Approximately 466 participants will be enrolled into this study.

Study identification

NCT ID
NCT06917404
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Enrollment
466 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
May 29, 2025 (Actual)
Primary completion
Jul 2027 (Estimated)
Completion
Jul 2027 (Estimated)
Last update posted
Sep 1, 2026

2025 – 2027

United States locations

U.S. sites
41
U.S. states
11
U.S. cities
37
Facility City State ZIP Site status
Onyx Clinical Research-Peoria Peoria Arizona 85381 —
Del Sol Research Management, LLC Tucson Arizona 85715 —
Orange County Research Institute Anaheim California 92801 —
Core Healthcare Group Cerritos California 90703 —
Triwest Research Center Chula Vista California 91910 —
Seaside Medical Group Oceanside California 92058 —
Paragon RX Clinical Santa Ana California 92703 —
Encompass Clinical Research Spring Valley California 91978 —
Focus Clinical Research West Hills California 91307 —
Clinical Research of West Florida - Clearwater Clearwater Florida 33765 —
GNP Research Cooper City Florida 33024 —
Arrow Clinical Trials Daytona Beach Florida 32117 —
AGA Clinical Trials Hialeah Florida 33012 —
Evolution Clinical Trials Miami Florida 33122 —
Well Pharma Medical Research Miami Florida 33173 —
K2 Medical Research Orlando Florida 32806 —
Progressive Medical Research Port Orange Florida 32127 —
Phoenix Clinical Research Tamarac Florida 33321 —
Conquest Research Winter Park Florida 32789 —
Chicago Clinical Research, Inc Chicago Illinois 60607 —
Northwestern University Chicago Illinois 60611 —
Sinai Hospital of Baltimore Baltimore Maryland 21215 —
Profound Research Farmington Hills Michigan 48334 —
Insight Research Institute Flint Michigan 48507 —
Rochester Medical Group Rochester Hills Michigan 48307 —
Onyx Clinical Research - Rochester Hills Troy Michigan 48085 —
Physician Research Collaboration Lincoln Nebraska 68516 —
Alpine Healthcare Family Practice Las Vegas Nevada 89109 —
Drug Trials America Hartsdale New York 10530 —
Groth Pain & Spine - Long Island, NY Mineola New York 11501 —
IMA Clinical Research Manhattan New York New York 10036 —
Groth Pain and Spine Management Smithtown New York 11787 —
FutureSearch Trials of Neurology Austin Texas 78731 —
FutureSearch Trials of Dallas Dallas Texas 75251 —
El Paso Clinical Trials El Paso Texas 79935 —
Vilo Research Group Houston Texas 77017 —
DM Clinical Research Houston Texas 77065 —
Clinical Trial Network Houston Texas 77074 —
Epic Clinical Research Lewisville Texas 75057 —
Quality Research Inc. San Antonio Texas 78209 —
Rio Clinical Trials Ogden Utah 84404 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06917404, 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, 2026 · Synced Nov 8, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06917404 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →