Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator
NCT03876054
Recruiting
The REALITY study is a prospective, post-market, non-randomized, multi-center, single-arm, open-label study intended to collect short- and long-term safety and effectiveness data on various populations implanted with Abbott's neurostimulation systems.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/19/2024
Locations: Phoenician Centers for Research & Innovation, Phoenix, Arizona +54 locations
Conditions: Chronic Pain
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d-Limonene +Radiation +Platinum Based Chemo for Xerostomia Prevention in Locally Advanced Head and Neck Squamous Cell Carcinoma
NCT04392622
Recruiting
This study explores the safety of d-limonene, a commercially-available dietary supplement (food) as a potential therapeutic for the severe dry mouth (xerostomia) experienced by patients with head and neck cancer as a side effect of their anti-cancer treatment.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/19/2024
Locations: Stanford University, Stanford, California
Conditions: Xerostomia
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CureDuchenne Link®: A Resource for Research
NCT04972604
Recruiting
CureDuchenne link is a data hub comprised of integrated biospecimens, clinical data, and self- and/or caregiver-reported information from participants. Anyone over 4 weeks old who has been diagnosed with DMD or BMD or who is a carrier of DMD or BMD can join. Parents or legal guardians can sign up their child(ren).
Gender:
ALL
Ages:
4 weeks and above
Trial Updated:
08/19/2024
Locations: Arkansas Children's Hospital, Little Rock, Arkansas +9 locations
Conditions: Duchenne Muscular Dystrophy, Becker Muscular Dystrophy
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IUD Self-Removal Study
NCT05339555
Recruiting
This is a pilot study designed to test the effectiveness of several techniques for intrauterine device (IUD) self-removal and to understand patient preferences regarding IUD self-removal and indicators of success as well as understanding the impacts of IUD self-removal on other clinical care.
Gender:
FEMALE
Ages:
Between 18 years and 50 years
Trial Updated:
08/19/2024
Locations: Oregon Health & Science Univeristy, Portland, Oregon
Conditions: IUD
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Exposure-Based CBT for Avoidant/Restrictive Food Intake in Functional Dyspepsia
NCT05587127
Recruiting
Randomized controlled trial of an exposure-based behavioral treatment (CBT) in adults with functional dyspepsia who meet criteria for avoidant/restrictive food intake disorder (ARFID) with weight loss.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/19/2024
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Avoidant/Restrictive Food Intake Disorder, Dyspepsia, Feeding and Eating Disorders, Cognitive Behavioral Therapy, Appetite Regulation, Functional Dyspepsia, Post-prandial Distress Syndrome, Behavioral Medicine
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P-CD19CD20-ALLO1 Allogeneic CAR-T Cells in the Treatment of Subjects With B Cell Malignancies
NCT06014762
Recruiting
Phase 1 study comprised of open-label, dose escalation and expansion cohort study of P-CD19CD20-ALLO1 allogeneic T stem cell memory (Tscm) CAR-T cells in subjects with relapsed/refractory B cell malignancies
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/19/2024
Locations: University of California San Diego, La Jolla, California +8 locations
Conditions: Primary Mediastinal Large B-cell Lymphoma (PMBCL), Diffuse Large B-Cell Lymphoma, Not Otherwise Specified, High-grade B-cell Lymphoma, Transformed Follicular Lymphoma (tFL), Follicular Lymphoma Grade 3B
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Orthopaedic Manual Physical Therapy as Part of the Postpartum Care Continuum
NCT06560190
Recruiting
Data shows us that injury risk increases in the first year postpartum. There is a paucity of literature regarding MSK injuries in postpartum military women. A unique challenge that postpartum service members face is the increased stress of training for and having to pass a physical fitness test directly tied to their career advancement. While there is epidemiological data across multiple branches of service, there is a gap in the literature in terms of how to appropriately address these decreas... Read More
Gender:
FEMALE
Ages:
Between 18 years and 44 years
Trial Updated:
08/19/2024
Locations: Brooke Army Medical Center, San Antonio, Texas
Conditions: Postpartum, Pregnancy Related
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Childhood Cancer Survivor Study
NCT01120353
Recruiting
The Childhood Cancer Survivor Study (CCSS) will investigate the long-term effects of cancer and its associated therapies. A retrospective cohort study will be conducted through a multi-institutional collaboration, which will involve the identification and active follow-up of a cohort of approximately 50,000 survivors of cancer, diagnosed before 21 years of age, between 1970 and 1999 and 10,000 sibling controls. This project will study children and young adults exposed to specific therapeutic mod... Read More
Gender:
ALL
Ages:
All
Trial Updated:
08/19/2024
Locations: University of Alabama at Birmingham/Children's of Alabama, Birmingham, Alabama +30 locations
Conditions: Cancer
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Thinking Zinc: a Study of Zinc Supplements on the Navajo Nation
NCT03908736
Recruiting
This is a study to assess the effect of dietary zinc supplementation to mitigate biomarkers of metal toxicity in exposed tribal populations.
Gender:
ALL
Ages:
Between 21 years and 64 years
Trial Updated:
08/19/2024
Locations: University of New Mexico Health Sciences Center, Albuquerque, New Mexico
Conditions: DNA Damage, Immune System Disorder
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Multicenter Outcome Registry of AnaLgesic Effect of SCS(MORALES) Registry Protocol
NCT04548375
Recruiting
The objective is to provide information to help the physician community decide the most effective type of device/therapy that would work for their patients, based off of the etiology of pain, the location of the pain for sustained pain relief.
Gender:
ALL
Ages:
All
Trial Updated:
08/19/2024
Locations: Summit Surgery Center, Reno, Nevada
Conditions: SCS
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Psilocybin-Enhanced Psychotherapy for Methamphetamine Use Disorder
NCT04982796
Recruiting
This is a proof-of-concept randomized clinical trial of psilocybin-enhanced psychotherapy versus treatment-as-usual among individuals being treated for methamphetamine use disorder.
Gender:
ALL
Ages:
Between 25 years and 65 years
Trial Updated:
08/19/2024
Locations: Portland VA Health Care System, Vancouver, Washington
Conditions: Amphetamine-Related Disorders
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A Diagnostic for the Early Detection of Bladder Cancer
NCT05347342
Recruiting
To improve upon the non-invasive detection of bladder cancer by further validating a multiplex ELISA assay directed at a bladder cancer-associated diagnostic signature in voided urine samples of patients with a high risk of developing bladder cancer.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
08/19/2024
Locations: Long Beach VA Healthcare System, Long Beach, California +1 locations
Conditions: Bladder Cancer
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