Clinical Trials Logo

Other clinical trials

View clinical trials related to Other.

Filter by:

NCT ID: NCT04337268 Completed - Clinical trials for The GLP-1-mediated Gut-kidney Axis

Acute Effects of GLP-1 on Renal Hemodynamics

GLP1RRBF
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

This study investigates the hypothesis, that GLP-1's suppression of ANG II and natriuretic action increase medullary perfusion and decrease oxygen consumption, leading to higher tissue oxygenation.

NCT ID: NCT04337203 Completed - Cancer Clinical Trials

Shared Healthcare Actions and Reflections Electronic Systems in Survivorship

Start date: September 8, 2020
Phase: N/A
Study type: Interventional

The primary purpose of this study is conduct a pilot study testing the study protocols, implementation program, and mixed-methods data collection.

NCT ID: NCT04336891 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Effect of Testosterone Treatment on Clitoral Arteries' Hemodynamic Parameters.

TESTOFSD
Start date: March 20, 2019
Phase:
Study type: Observational

The regulation of clitoral vascularization by sex steroids is still under-investigated. We aimed to explore the effects of 6 months transdermal Testosterone (T) therapy on clitoral color Doppler ultrasound (CDU) parameters in pre- and postmenopausal women with female sexual dysfunction (FSD). In order to do that, we retrospectively recruited n=81 women with FSD, divided into 4 groups according to different treatments followed as per clinical practice, for 6 months: transdermal systemic 2% T gel; local estradiol ovules; local non-hormonal moisturizers; transdermal T plus local estrogens. Our main hypothesis is that systemic T treatment is able to positively modulate clitoral blood flow in basal conditions, specifically to increase clitoral artery Peak systolic velocity (PSV).

NCT ID: NCT04336826 Completed - Clinical trials for Nonsene Mutation Duchenne Muscular Dystrophy

A Study to Evaluate the Safety and Pharmacokinetics of Ataluren in Participants From ≥6 Months to <2 Years of Age With Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)

Start date: December 29, 2021
Phase: Phase 2
Study type: Interventional

This study is designed to evaluate safety, tolerability, and pharmacokinetics (PK) in male children with nmDMD aged ≥6 months to <2 years treated daily for 24 weeks with orally administered ataluren 10, 10, and 20 milligrams/kilogram (mg/kg) (morning, mid-day, and evening dose, respectively).

NCT ID: NCT04336800 Completed - Clinical trials for Diabetes Mellitus, Type 2

Multi-Parametric MRI Assessment of the Liver in Diabetic Volunteers (Partners Registry)

Start date: April 1, 2020
Phase:
Study type: Observational

To build a registry of diabetic volunteers by inviting them to get a LiverMultiScan and collecting their contact information to seek interest in participating in future research studies.

NCT ID: NCT04336618 Completed - Clinical trials for Non-Alcoholic Fatty Liver Disease

Multi-Parametric MRI Assessment of the Liver in the Dallas-FortWorth Metroplex Population

DFWRegistry
Start date: August 3, 2020
Phase:
Study type: Observational

To build a Registry of volunteers by inviting them to get a LiverMultiScan(LMS)and collecting their contact information to seek interest in participating in future studies.

NCT ID: NCT04336592 Completed - Clinical trials for Non-Pharmacological Pain Management

Pain Management Intervention Preparatory to a Future Pragmatic Trial

Start date: May 13, 2020
Phase:
Study type: Observational

Researchers are promoting non-pharmacological pain management strategies for patients by assisting them in identifying post-surgical pain care preference following an operative procedure at Mayo Clinic.

NCT ID: NCT04336345 Completed - COVID-19 Clinical Trials

Outcomes of Patients With COVID-19 in the Intensive Care Unit

MexCOVID-19
Start date: April 1, 2020
Phase:
Study type: Observational [Patient Registry]

The objective of this study is to evaluate the clinical characteristics and outcomes of critically ill patients with COVID-19 admitted to the intensive care unit. A Multicenter Observational Study.

NCT ID: NCT04336085 Completed - Clinical trials for Post Operative Pain After Pediatric Hip Surgery

Comparison of Ultrasound Guided Caudal Block and Ultrasound Guided Pericapsular Nerve Group Block for Pediatric Hip Surgery

Start date: April 15, 2020
Phase: N/A
Study type: Interventional

Surgical repair of the hip can be extremely painful and is associated with considerable postoperative pain in children despite the use of systemic opioids. These patients may benefit from neuraxial analgesia in adjunction with general anesthesia. The reported advantages of this technique include decreased opiate exposure, decreased time in the post-anesthesia recovery room, decreased hospital stay, reduce the post-operative morbidity, provide early mobilization. Ultrasound guided caudal block has many advantages as it is helpful for visualization of the sacral hiatus, sacrococcygeal ligament, epidural space and the distribution of the local anesthetic agent within the epidural space. So, the success rate of caudal block is increase . Pericapsular nerve group (PENG) block has been recently recommended by Girón-Arango et al. for use as postoperative analgesia in hip surgeries (8) It is a new regional anesthesia method in the region between the anterior inferior iliac spine (AIIS) and ilio-pubic eminence

NCT ID: NCT04336072 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Reminder Focused Positive Psychiatry in Adolescents With ADHD and PTSD

Start date: January 10, 2017
Phase: N/A
Study type: Interventional

This feasibility study investigates the impact of reminder-focused-positive-psychiatry (RFPP) on attention-deficit-hyperactive-disorder (ADHD) and posttraumatic-stress-disorder (PTSD) symptoms, vascular-function, inflammation and well-being of adolescents with comorbid ADHD & PTSD. In this randomized clinical trial, 24 subjects with comorbid ADHD and PTSD, aged 12-18 years old, free of known medical and other major psychiatric disorders, will be recruited from the pool of eligible subjects at Los Angeles and Kern County Children Mental Health Centers (>1500 subjects) after obtaining informed consent from parents as well as subjects' assentment. Commonwealth and Oswell Kern County Mental Health Clinic will be used for subjects enrollment, randomization as well as study implementation from trauma disorder clinic. Kern Medical will be used for manuscript write up and analyses. Adolescents will be randomized to: group-RFPP or trauma-focused group-cognitive-behavioral-therapy (TF-CBT). Participants will complete twice-weekly-intervention for 6-weeks-trial. The group-RFPP-intervention will be inclusive of RFPP interventions on a) traumatic-reminders, and b Avoidance & negative-cognition. Vascular-function-measured as temperature-rebound (TR), C-reactive-protein (CRP), homocysteine, SNAP-questionnaire, Clinician-Administered PTSD-Scale-children-version (CAPS-CA) and neuropsychiatric-measures will be measured at baseline and 6th week. Subjects will be followed for 12 months. Parents and subjects will be informed of the risks associated with use of venipuncture and loss of confidentiality of collected information.