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NCT ID: NCT05981794 Recruiting - Pain Clinical Trials

Heating Pad for in Office Cystoscopy and Urodynamic Testing

Start date: January 3, 2024
Phase: N/A
Study type: Interventional

Patient frequently report experiencing discomfort associated with cystoscopy or urodynamic studies (UDS), and a small percentage of patients refuse these important procedures due to discomfort or fear of discomfort. Heating pads are an inexpensive and low-risk way to reduce patient discomfort during these procedures, which to our knowledge has not been investigated in the United States.

NCT ID: NCT05981755 Recruiting - Focal Epilepsy Clinical Trials

Breathing Rescue for SUDEP Prevention

BreatheS
Start date: July 31, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to precisely delineate human brain networks that modulate respiration and identify specific brain areas and stimulation techniques that can be used to prevent seizure-induced breathing failure.

NCT ID: NCT05981716 Recruiting - Breast Cancer Clinical Trials

Young Breast Cancer Survivors Study

YBCSS
Start date: January 10, 2023
Phase:
Study type: Observational

Despite significant overall reductions in mortality rates for breast cancer over the past decade, both incidence and mortality rates have steadily climbed in adults diagnosed before age 50. This research project addresses factors associated with quality of life among and treatment response in early-age-at-onset breast cancer patients. The overall objective is collect information from early-onset breast cancer patients using an online questionnaire and examine factors related to cancer survival, (i.e.,better quality of life, better treatment adherence, less adverse treatment responses). Aim 1: Identify dietary patterns related to health-related quality of life in early-age-at-onset breast cancer patients. The investigators hypothesize that diet quality is related to better health-related quality of life among young breast cancer survivors. Aim 2. Identify demographic, social determinants, and geographic factors associated with treatment adherence. The investigators hypothesize that social determinants such as poverty-to-income ratio, education, and proximity to cancer treatment facilities are associated with treatment adherence in early-onset breast cancer.

NCT ID: NCT05981703 Recruiting - Solid Tumor Clinical Trials

A Study Investigating BGB-26808 Alone or in Combination With Tislelizumab in Participants With Advanced Solid Tumors

Start date: September 7, 2023
Phase: Phase 1
Study type: Interventional

This is an open-label, multicenter, and nonrandomized dose escalation and dose expansion study to evaluate BGB-26808 as monotherapy or in combination with tislelizumab in participants with advanced solid tumors. The main purpose of this study is to explore the recommended dosing for BGB-26808.

NCT ID: NCT05981573 Recruiting - Pain, Chronic Clinical Trials

Assessment of Methadone Dose Taken Using Electrochemistry

Start date: June 2024
Phase:
Study type: Observational

Proof of concept: Pilot Study A Pilot, proof of concept, observational study with a long-term goal to develop a minimally invasive wearable Remote Medication Monitor (RMM) that provides continuous, real-time data on methadone levels in interstitial fluid (ISF). An RMM could be used as a medication adherence monitor and would allow for the physician, counselor, patient, or family member to remotely verify that a physician-prescribed dose has been taken.

NCT ID: NCT05981508 Recruiting - Obesity Clinical Trials

Online Family Dyadic Skills Training for Black Adults in Behavioral Weight Loss Program

TEAM+
Start date: February 5, 2024
Phase: N/A
Study type: Interventional

The purpose of this research study is to test the feasibility and acceptability of an interactive counselor -led online family skills training as part of a behavioral weight loss program for Black Adults.

NCT ID: NCT05981443 Recruiting - Surgical Wound Clinical Trials

An Analysis of Dermabond vs. Non-Absorbable Sutures in Skin Closure for Brow Ptosis Procedures

Start date: August 15, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare Dermabond with non-absorbable sutures in skin closure after brow ptosis surgery. The main questions it aims to answer are: - if Dermabond provides equivalent wound healing compared to conventional non-absorbable skin suture techniques - if Dermabond provides equivalent scar appearance compared to conventional non-absorbable suture techniques - if Dermabond results in equivalent complication rates compared to conventional non-absorbable suture techniques Participants will have be randomly selected to have either Dermabond or non-absorbable suture closure methods. Scar analysis and both participant and provider surveys will be performed to assess the differences between groups, if any.

NCT ID: NCT05981391 Recruiting - Clinical trials for Posttraumatic Stress Disorder

Neurobiological Similarities of Tinnitus and PTSD

Start date: February 4, 2021
Phase:
Study type: Observational

Psychiatric distress caused by PTSD may increase attention toward tinnitus, as well as perceived loudness and discomfort. It is important to understand how tinnitus-related distress and PTSD negatively interact together, in order to develop more effective therapeutic approaches. Understanding symptoms and neurobiological mechanisms using functional magnetic resonance imaging (fMRI), can lead to the necessary knowledge to develop effective interventions for individuals who suffer from both conditions.

NCT ID: NCT05981365 Completed - Sickle Cell Disease Clinical Trials

Voxelotor CYP and Transporter Cocktail Interaction Study

Start date: April 17, 2023
Phase: Phase 1
Study type: Interventional

This research study is examining multiple doses of voxelotor (a study drug intended for treatment of sickle cell disease) and how it interacts with additional substrates (substrates are drugs or other substances that are metabolized by cytochrome enzymes. The substrates used in this study are FDA approved medications). The study will help to determine the safety and tolerability of the study drugs taken together, as well as the pharmacokinetics (PK) on how your body processes and responds to the combination of the study drug and substrates. Although these drugs are FDA approved, their use in this study is experimental.

NCT ID: NCT05981300 Not yet recruiting - Gastroparesis Clinical Trials

GpCRC Pediatric Gastroparesis Registry 2

PGpR2
Start date: June 30, 2024
Phase:
Study type: Observational [Patient Registry]

The objective of the Pediatric Gastroparesis Registry 2 is to create a national prospective registry of children, adolescents, and young adults with gastroparesis and gastroparesis-like syndrome (symptoms of gastroparesis but normal gastric emptying).