The state of Kansas currently has 21 active clinical trials seeking participants for Pain research studies. These trials are conducted in various cities, including Wichita, Kansas City, Overland Park and Topeka.
Trial Readiness and Endpoint Assessment in LGMD R1
NCT05618080
Recruiting
This is a 24-month, observational study of 100 participants with Limb Girdle Muscular Dystrophy type R1, also known as CAPN3.
Gender:
All
Ages:
Between 12 years and 50 years
Trial Updated:
02/01/2024
Locations: University of Kansas Medical Center, Kansas City, Kansas
Conditions: Calpain-3 Deficiency Limb Girdle Muscular Dystrophy Type 2A, Limb Girdle Muscular Dystrophy, Limb Girdle Muscular Dystrophy Type R1, LGMD2A
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Comparison of Qutenza (8% Capsaicin) With a Low-dose Capsaicin for Treatment of Nerve Pain After Surgery
NCT04967664
Recruiting
This is an interventional, Phase III, double-blind, randomized, controlled, parallel-group, multi-site, clinical trial to confirm the efficacy and safety of repeated topical application of Qutenza (capsaicin 8% topical system) versus low-dose capsaicin control (capsaicin 0.04% topical system) in subjects with moderate to severe postsurgical neuropathic pain (PSNP).
Gender:
All
Ages:
18 years and above
Trial Updated:
12/05/2023
Locations: Neuroscience Research Center, LLC, Overland Park, Kansas +1 locations
Conditions: Post Surgical Neuropathic Pain
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Chronic Pain, Opioid Use, and Epidermal Nerve Fiber Density
NCT04801498
Recruiting
This pilot study is being performed to examine whether epidermal axons are altered in patients taking opioid therapy for chronic non-cancer pain, and if epidermal axonal changes predict heightened pain sensitivity.
Gender:
All
Ages:
Between 18 years and 65 years
Trial Updated:
12/01/2023
Locations: University of Kansas Health System, Kansas City, Kansas
Conditions: Chronic Pain, Opioid Use, Nerve Disorders
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A Dose-Finding Study to Evaluate the Efficacy and Safety of GSK3858279 in Adults With Knee Osteoarthritis Pain
NCT05838742
Recruiting
This is dose-finding study of GSK3858279 in participants with moderate to severe knee osteoarthritis (OA) pain. The purpose of this study is to investigate and provide the data necessary to select the optimal effective and safe dose(s) of GSK3858279.
Gender:
All
Ages:
Between 40 years and 80 years
Trial Updated:
10/11/2023
Locations: GSK Investigational Site, Wichita, Kansas
Conditions: Pain
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Quantify the Degree of Pain Relief of Pelvic Congestion Syndrome Following Gonadal Vein Embolization
NCT03794466
Recruiting
The primary objective is to quantify the degree of pain relief in patients undergoing gonadal vein embolization with coils as well as identify clinical or imaging factors that are predictive of a positive response to treatment, or poor response to treatment.
Gender:
Female
Ages:
18 years and above
Trial Updated:
07/28/2023
Locations: The University of Kansas Medical Center, Kansas City, Kansas
Conditions: Pelvic Congestive Syndrome, Pelvic Pain
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A Phase 1, Randomized, Placebo-Controlled Safety and Tolerability Study Of Intravenous SBS-1000 in Healthy Adults
NCT05721287
Recruiting
This study will be a single-center, double-blind, randomized placebo-controlled, adaptive, single ascending dose study.
Gender:
All
Ages:
Between 18 years and 59 years
Trial Updated:
01/31/2023
Locations: Altasciences Clinical Kansas, Overland Park, Kansas
Conditions: Pain, Acute Pain
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Improving Pain Management Via Spinal Cord Stimulation and Blood Pressure Reduction
NCT04676399
Recruiting
The purpose of this study (PASSION study) is to monitor symptoms of chronic pain before and after 2 weeks of a standard drug commonly used to treat elevated blood pressure compared with 2 weeks of placebo (crossover design) so that we may better understand how blood pressure affects your level of pain. This study is not testing an experimental drug.
Gender:
All
Ages:
Between 40 years and 79 years
Trial Updated:
02/08/2022
Locations: The Marc A. Asher Comprehensive Spine Center at the Kansas University Medical Center, Kansas City, Kansas
Conditions: Chronic Pain, Hypertension, Diuretics Drug Reactions, SCS
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Evaluation of Multi-Tined Expandable Electrode (MEE) Efficacy and Safety in Treatment of Lumbar Facet Arthropathy by Radiofrequency Neurotomies Compared to Conservative Medical Management.
NCT04730700
Recruiting
The purpose of this study is to better understand how people feel after a radiofrequency ablation standard of care surgery using a different type of needle (multi-tined expandable electrode/MEE) in comparison to receiving conventional medical management (CMM) techniques.
Gender:
All
Ages:
18 years and above
Trial Updated:
05/06/2021
Locations: University of Kansas Medical Center, Kansas City, Kansas
Conditions: Chronic Low-back Pain
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Epidural Spinal Cord Stimulation for Hypertension in Patients With Neuropathic Pain
NCT04598035
Recruiting
The purpose of the ESCAPE Study is to determine the extent to which epidural spinal cord stimulation (SCS) reduces arterial blood pressure (BP) in patients which chronic low back pain and hypertension. We also aim to determine the extent to which higher baseline BP (i.e., hypertension) predicts reductions in pain following SCS implant. This is an observational study of patients undergoing an implantation of a SCS device.
Gender:
All
Ages:
Between 30 years and 89 years
Trial Updated:
01/28/2021
Locations: University of Kansas Clinical and Translational Science Unit (CTSU), Fairway, Kansas +1 locations
Conditions: Chronic Pain, Hypertension, Implanted Stimulation Electrodes
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