Crisis Response Planning for Military Personnel
NCT05795764
Recruiting
The study is a randomized trial comparing outcomes of active duty service members who present to the emergency department at risk for suicide and receive care from providers trained in crisis response planning versus those providing treatment as usual.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: Naval Medical Center San Diego, San Diego, California
Conditions: Suicidal, Suicide Threat, Suicidal Ideation
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Blood Specimen Collection For Laboratory Assay Research
NCT06046651
Recruiting
To collect lab data from capillary and venous blood specimens for use in analytical research studies to support the development and validation of laboratory procedures.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: Roman Health Ventures Study Site, San Francisco, California
Conditions: General; Metabolic Disorder, Sexual Dysfunction, Hair Loss, Pathology
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Study of Acute Normovolemic Hemodilution (ANH) in People with Ovarian Cancer Who Are Having Cytoreductive Surgery
NCT06290193
Recruiting
Participants will be scheduled for primary cytoreductive surgery as part of their standard care. Before surgery, participants will be assigned by chance to a study group. Depending on which group they are in, they will receive either acute normovolemic hemodilution/ANH during surgery or standard surgical management during surgery. The researchers think acute normovolemic hemodilution/ANH may decrease the need for allogenic blood transfusion/ABT in people having primary cytoreductive surgery.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: Memoral Sloan Kettering at Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey +6 locations
Conditions: Ovarian Cancer, Fallopian Tube Carcinoma, Ovarian Carcinoma, Peritoneal Carcinoma, Ovarian Cancer Stage IIIC, Fallopian Tube Cancer Stage IIIC, Ovarian Cancer Stage IV, Fallopian Tube Cancer Stage IV, Fallopian Tube Cancer, Peritoneal Cancer
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Training for Urinary Leakage Improvement After Pregnancy
NCT06411158
Recruiting
This is a multi-center, randomized single-blind nonsurgical trial conducted in approximately 216 primiparous postpartum women at high risk for prolonged/sustained pelvic floor disorders with symptomatic, bothersome urinary incontinence (UI) amenable to nonsurgical treatment. TULIP is a 3-Arm trial with two active interventions (Arms 1 and 2) and a Patient Education control arm (Arm 3). Arm 1 consists of pelvic floor muscle training (PFMT). Arm 2 uses a home biofeedback device (leva®). The prim... Read More
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: Kaiser Permanente -- San Diego, San Diego, California +6 locations
Conditions: Urinary Incontinence, Delivery Complication
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PK/PD of Digoxin in Infants With SVHD
NCT06613477
Recruiting
The primary participant will be an infant with single ventricle heart disease. This is a research study to learn more about how the medication digoxin, which is routinely prescribed to infants and children with heart disease in pediatric cardiac intensive care units is processed by their bodies and how it may help their cardiac function. The investigators will collect blood or will collect blood samples when bloodwork is checked as part of regular care ("opportunistic"). The investigators will... Read More
Gender:
ALL
Ages:
Between 30 days and 6 months
Trial Updated:
11/13/2024
Locations: Duke University Medical Center, Durham, North Carolina +1 locations
Conditions: Single-ventricle, Infant Conditions, Infant, Newborn, Diseases, Infant, Premature, Diseases
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Atypical Hemolytic-Uremic Syndrome (aHUS) Registry
NCT01522183
Recruiting
Post-marketing safety data on patients treated and untreated with eculizumab or ravulizumab.
Gender:
ALL
Ages:
All
Trial Updated:
11/13/2024
Locations: Clinical Trial Site, Aurora, Colorado +137 locations
Conditions: Atypical Hemolytic-Uremic Syndrome
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Safety and Efficacy of ActiGraft Treatment in Wound Care in Medical Centers
NCT04699305
Recruiting
Multicenter observational study to explore the efficacy of ActiGraft in the treatment of exuding cutaneous wounds in real-life usage.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: Wound Care Experts, Las Vegas, Nevada
Conditions: Cutaneous Wounds
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Effects of Immulina TM Supplements with PASC Patients
NCT05524532
Recruiting
This is a multi-site study that will try to determine the effects of Immulina ™, a natural dietary supplement, on blood chemicals associated with inflammation that are often increased in patients with long COVID (also called PASC).
Gender:
ALL
Ages:
Between 18 years and 99 years
Trial Updated:
11/13/2024
Locations: University of Hawaii, Honolulu, Hawaii +8 locations
Conditions: Post Acute COVID-19 Syndrome
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An Evaluation of an Online Sexual Assault Resistance Program (IDEA3)
NCT06058455
Recruiting
The goal of this randomized trial is to test whether the Internet-Delivered Enhanced Assess, Acknowledge, Act (IDEA3) sexual assault resistance education intervention reduces sexual violence victimization in undergraduate women. Participants in the intervention group will be asked to attend four three-hour group sessions of a sexual assault resistance program called IDEA3 with a partner, as well as fill out a number of surveys. Participants in the control group will be asked to attend a one-hou... Read More
Gender:
ALL
Ages:
Between 17 years and 24 years
Trial Updated:
11/13/2024
Locations: University of Michigan, Ann Arbor, Michigan +3 locations
Conditions: Sexual Assault
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A Comparative Clinical Study to Assess Pain Score and Wound Healing Following Fractional Ablation With a DFG Laser and CO2 Laser
NCT06295471
Recruiting
This research study aims assess whether the Difference Frequency Generation (DFG) laser could be a better alternative to the CO2 laser in terms of reduced side effects and patient downtime.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: MGH Clinical Unit for Research Trials & Outcomes in Skin, Boston, Massachusetts
Conditions: Healthy
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Joining Under-connected Networks to Optimize "Salud" (Health) ("JUNTOS")
NCT06432725
Recruiting
The objective of this study is to evaluate the JUNTOS Referral Network as an implementation strategy to enhance the reach of HIV-prevention and treatment services to Latino gay, bisexual, and other men who have sex with men (MSM).
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: University of Miami, Coral Gables, Florida
Conditions: Hiv
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Continuous Glucose Monitors (CGMs) for All: Studying the Impact of Expanding CGM Access
NCT06658067
Recruiting
This non-blinded, non-randomized pre-post study will examine the impact of providing CGM sensors free of charge to adult patients of Fair Haven Community Health Care with poorly controlled type 2 diabetes on glycemic control and quality of life.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
11/13/2024
Locations: Fair Haven Community Health Care (FHCHC), New Haven, Connecticut
Conditions: Diabetes, Type 2 Diabetes, Type 2 Diabetes Mellitus - Poor Control
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