🔎 Trials Near Me

Home › Knee Osteoarthritis › NCT05986292

A Master Protocol Study (LY900028) of Multiple Intervention-Specific-Appendices (ISAs) in Participants With Chronic Pain

RecruitingPhase 2

A Master Protocol for Randomized, Placebo-Controlled, Phase 2 Clinical Trials of Multiple Interventions for the Treatment of Chronic Pain

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* have a visual analog scale (VAS) pain value ≥40 and \<95 at screening and prerandomization screening.
* have a history of daily pain for at least 12 weeks based on participant report or medical history
* have a value of ≤30 on the pain catastrophizing scale
* are willing to maintain a consistent regimen of any ongoing nonpharmacologic pain-relieving therapies (for example, physical therapy) and/or nutritional supplements and will not start any new nonpharmacologic pain-relieving therapies and/or nutritional supplements during study participation
* are willing to discontinue all medications taken for chronic pain conditions, except rescue medication for the duration of the study

Exclusion Criteria:

* have second- or third-degree atrioventricular (AV) heart block or AV dissociation or history of ventricular tachycardia
* have had a procedure within the past 6 months intended to produce permanent sensory loss in the target area of interest (for example, ablation techniques)
* have surgery planned during the study for any reason, related or not to the disease state under evaluation.
* have, in the judgment of the investigator, an acute, serious, or unstable medical condition or a history or presence of any other medical illness that would preclude study participation.
* have had cancer within 2 years of baseline, except for cutaneous basal cell or squamous cell carcinoma resolved by excision.
* have fibromyalgia
* have any clinically important abnormality at screening, as determined by investigator, in physical or neurological examination, vital signs, electrocardiogram (ECG), or clinical laboratory test results that could be detrimental to the participant or could compromise the study.
* have a positive human immunodeficiency virus (HIV) test result at screening
* have a history of alcohol, illicit drug, analgesic or narcotic use disorder within 2 years prior to screening.

About the study

The purpose of the chronic pain master protocol is to compare independent pain interventions and establish an overarching structure for the disease-state addenda (DSA) and intervention-specific appendices (ISAs). The ISAs may start independently of other ISAs as interventions become available for clinical testing.

What is being tested

Sponsor: Eli Lilly and Company · Participants: 10,000 · Started: Jan 30, 2020

Contact the study team

Official record on ClinicalTrials.gov — NCT05986292

Locations in the U.S.

AlabamaCentral Research Associates, Birmingham
ArizonaArizona Research Center, Phoenix
Synexus Clinical Research US, Inc., Phoenix
CaliforniaDesert Oasis Healthcare Medical Group, Palm Springs
Artemis Institute for Clinical Research, Riverside
Artemis Institute for Clinical Research, San Diego
ConnecticutCMR of Greater New Haven, LLC, Hamden
FloridaBradenton Research Center, Inc., Bradenton
Clinical Research of South Florida, Coral Gables (Not yet recruiting)
Accel Research Sites - DeLand Clinical Research Unit, DeLand
K2 MEDICAL Research THE VILLAGES, Lady Lake
K2 Medical Research ORLANDO, Maitland
Merritt Island Medical Research, LLC, Merritt Island
Flourish Research - Miami, LLC, Miami
New Horizon Research Center, Miami
University of Miami Don Suffer Clinical Research Building, Miami (Not yet recruiting)
Suncoast Clinical Research, Inc., New Port Richey
Renstar Medical Research, Ocala
Synexus Clinical Research US, Inc., Orlando (Not yet recruiting)
Precision Clinical Research, Sunrise
Charter Research - Lady Lake, The Villages
Conquest Research, Winter Park
GeorgiaNorth Georgia Clinical Research, Woodstock
IdahoRocky Mountain Clinical Research, Idaho Falls (Not yet recruiting)
IllinoisNorthwestern University, Chicago
LouisianaDelRicht Research, New Orleans
MassachusettsBoston Clinical Trials, Boston (Not yet recruiting)
Lucida Clinical Trials, New Bedford
MedVadis Research Corporation, Waltham
MichiganGreat Lakes Research Group, Inc., Bay City
MissouriStudyMetrix Research, City of Saint Peters
Clinvest Research LLC, Springfield
New YorkRochester Clinical Research, LLC, Rochester
North DakotaLillestol Research, Fargo
OhioMETA Medical Research Institute, Dayton
OklahomaDelRicht Research, Tulsa
PennsylvaniaAltoona Center For Clinical Research, Duncansville
TexasFutureSearch Trials of Neurology, Austin
WashingtonNorthwest Clinical Research Center, Bellevue
Rainier Clinical Research Center, Renton

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.