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NCT ID: NCT04625634 Completed - Hyperthermia Clinical Trials

Simulation of Consecutive Day Shift Work

Start date: December 2, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine differences in physiological recovery between two consecutive days of simulated fire suppression work. The secondary purpose is to determine differences in heat gain and heat loss between two consecutive days of simulated fire suppression work. Subjects will complete two consecutive days of simulated structural firefighting shift work, 24 hours apart. Before and after each laboratory visit, subjects will continuously wear a Holter monitor and ambulatory blood pressure monitor to quantify parasympathetic tone and recovery from work.

NCT ID: NCT04625595 Completed - Type1 Diabetes Clinical Trials

Multiple Ascending Dose (MAD) Study of IMT-002 in HLA-DQ8-positive Type 1 Diabetes

Start date: November 9, 2020
Phase: Phase 1
Study type: Interventional

This study is designed to characterize the safety, steady-state pharmacokinetics (PK) of IMT-002, and will serve as a dose range identification for the pharmacodynamic effect of blocking self-antigen presentation in adults with type 1 diabetes (T1D) having the human leukocyte antigen (HLA)-DQ8 gene.

NCT ID: NCT04625504 Completed - Chronic Pain Clinical Trials

Investigating Biological Targets, Markers, and Intervention for Chronic Pain

Start date: November 25, 2020
Phase: N/A
Study type: Interventional

This multi-modal methods study will investigate neurophysiological, endocrinological, cognitive, psycho-social-emotional markers of chronic pain, and therapeutic targets using integrative health treatments.

NCT ID: NCT04625465 Completed - Clinical trials for Stress, Psychological

Proximal Effects of Alcohol on Same-Sex Intimate Partner Violence

PASSION
Start date: November 12, 2020
Phase: N/A
Study type: Interventional

We will recruit sexual and gender minority couples to complete 56 days of daily surveys in order to evaluate (1) the impact of COVID-19 stress and sexual and gender minority stress on heavy episodic drinking and intimate partner violence (IPV) perpetration, and (2) a brief, mobile-phone delivered text messaging intervention to mitigate the effects of these stressors. This project has high potential to inform how pandemic stress contributes to etiological models of alcohol-related IPV perpetration in sexual and gender minority couples and inform a culturally-sensitive, low burden, and easy to disseminate intervention to mitigate these effects critical during a pandemic when access to care is limited.

NCT ID: NCT04625439 Completed - Cancer Clinical Trials

Personality and Cancer Care Study

Start date: November 18, 2020
Phase: N/A
Study type: Interventional

This randomized clinical trial will test whether giving an individualized personality feedback report to adults with a history of cancer can improve their self-awareness, confidence in managing their illness, and mood.

NCT ID: NCT04625413 Completed - Clinical trials for Acute Myeloid Leukemia

A Patient-centered Communication Tool (UR-GOAL) for Older Patients With Acute Myeloid Leukemia, Their Caregivers, and Their Oncologists

Start date: October 23, 2021
Phase: N/A
Study type: Interventional

This is a pilot study to evaluate the usability and feasibility of a patient-centered communication tool (University of Rochester-Geriatric Oncology Assessment for acute myeloid Leukemia or UR-GOAL) among 15 older patients with AML, their caregivers, and oncologists.

NCT ID: NCT04625335 Completed - Pain Clinical Trials

Effects of Prophylactic Massage Therapy on Pain Tolerance and Threshold

Start date: September 1, 2015
Phase: N/A
Study type: Interventional

Therapeutic massage has been thought to reduce anxiety and increase relaxation in human patients.This study is meant to determine the immediate effects of therapeutic massage on pain tolerance and threshold.

NCT ID: NCT04625283 Completed - Anesthesia Clinical Trials

The Impact of Perioperative Ketamine Infusion on Surgical Recovery

Start date: April 12, 2021
Phase: Phase 4
Study type: Interventional

In order to effectively treat surgical pain with the least amount of opioids required, a multi-modal approach must include medications with different mechanisms of actions at alternative receptors. In light of the opioid epidemic, medical providers at Vanderbilt University Medical Center (VUMC) are strategically combining these medications in a bundled pain-regimen after surgery. These regimens have been shown to decrease opioid consumption, improve surgical outcomes, and reduce hospital stays, thus coining the term 'enhanced recovery pathway'. The combination of these medications has an indisputable synergistic effect. However, it is unknown how each medication contributes individually to the overall efficacy of the pathway. This study will examine the effects of ketamine, within the constructs of a multimodal pain regimen, on a) length of stay, b) opioid consumption, and c) surgical outcomes after major abdominal surgery.

NCT ID: NCT04625231 Completed - Surgery Clinical Trials

Shared Decision-Making Tool for Opioid Prescribing After Ambulatory Hand Surgery in Veterans

Start date: November 9, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if an educational patient-centered presentation reduced the amount of opioid pills requested and utilized by patients compared to standard of care group.

NCT ID: NCT04625101 Completed - Clinical trials for Epileptic Encephalopathy

Efficacy, Safety, Tolerability, and Pharmacokinetics of NBI-827104 in Pediatric Subjects With Epileptic Encephalopathy With Continuous Spike-and-Wave During Sleep

Start date: April 26, 2021
Phase: Phase 2
Study type: Interventional

This is a phase 2, double-blind study to assess the efficacy, safety, tolerability, and pharmacokinetics of NBI-827104 when administered once daily for 13 weeks in pediatric subjects with Epileptic Encephalopathy with Continuous Spike-and-Wave During Sleep (EECSWS).