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NCT ID: NCT04485728 Completed - Clinical trials for Sleep Disturbance in Hospitalized Antepartum Patients

Sleep Improvement Intervention for Hospitalized Antepartum Patients

Start date: March 11, 2022
Phase: N/A
Study type: Interventional

This project seeks to further study the effects of a hospital-based protocol for improving sleep in high-risk antepartum patients as piloted by Lee and Gay (2017).

NCT ID: NCT04485585 Completed - Overactive Bladder Clinical Trials

A Study to Evaluate Drug-drug Interactions Between BR9006-1 and BR9006-2 in Healthy Male Volunteers.

Start date: July 20, 2020
Phase: Phase 1
Study type: Interventional

To evaluate the influence of BR9006-1 and BR9006-2 on pharmacokinetics, safety, and tolerability when administered separately or co-administered to healthy male volunteers.

NCT ID: NCT04485572 Completed - Clinical trials for Radiculopathy, Lumbosacral Region

Diagnostic Validity of the Neurodynamic or Orthopedic Tension Tests

Start date: July 1, 2014
Phase:
Study type: Observational

The objective of the present study is to analyse the diagnostic validity of 8 neurodynamic and/or orthopedic tension tests using magnetic resonance imaging as the Gold Standard.

NCT ID: NCT04485520 Completed - Dental Plaque Clinical Trials

Efficacy of the Extract of Carica Papaya as an Inhibitor of Streptococcus Mutans

Start date: September 21, 2017
Phase: N/A
Study type: Interventional

Papaya has effects on oral pathogenic microorganisms, it also has anticoagulant quality, amebicidal action, antimicrobial, bacteriostatic and antifungal activity on different bacteria, especially on Streptococcus mutans, this can be exploited in the dental area. The objective of the study was to determine the efficacy of Carica Papaya peel extract (suckling) as an inhibitor of Streptococcus Mutans in students of the dental faculty of the National University of Caaguazú in 2018.

NCT ID: NCT04485234 Completed - Clinical trials for Coronary Artery Disease

Inclusive Invasive Physiological Assessment in Angina Syndromes Registry

ILIAS Registry
Start date: June 1, 2019
Phase:
Study type: Observational [Patient Registry]

This study evaluates the prognostic value and potential therapeutic impact of combined pressure and flow measurements in the evaluation of epicardial coronary stenosis and microvascular function.

NCT ID: NCT04484857 Completed - Clinical trials for Anemia Associated With End Stage Renal Disease

Study of Roxadustat Conversion in Participants Receiving Stable ESA or as Initial Anemia Treatment in Hemodialysis Participants

ASPEN
Start date: July 22, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and effectiveness of roxadustat dosing regimens among hemodialysis participants converted from erythropoiesis stimulating agent (ESA) therapy or who are ESA-naïve.

NCT ID: NCT04484805 Completed - Amputation Clinical Trials

Socket Cooling Effectiveness Take Home Study

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

The comfort and fit of the residual limb within a prosthetic socket are of primary concern for many amputees. The residual limb is typically covered by non-breathable and non- thermally conductive materials that can create a warm and ultimately moist environment. To address this, Liberating Technologies, Inc. (LTI) and Vivonics, Inc. have developed a thermo-electric cooling (TEC)-based module called the Intrasocket Cooling Element (ICE), that can be embedded into the prosthesis in order to cool the residual limb. A technology that can provide thermal control while retaining adequate suspension, weight and other prosthetic characteristics would benefit many prosthesis wearers.

NCT ID: NCT04484467 Completed - Clinical trials for Irritable Bowel Syndrome

Efficacy and Safety of a Food Supplement With Standardized Menthol, Limonene, and Gingerol Content in Patients With Irritable Bowel Syndrome

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

The purpose of this study is to assess the efficacy and safety of a food supplement with standardized menthol, limonene, and gingerol content in patients with irritable bowel syndrome (IBS) or IBS/functional dyspepsia (FD).

NCT ID: NCT04483947 Completed - Clinical trials for Non-alcoholic Steatohepatitis (NASH)

A Study to Assess Safety, Tolerability, PK and PD of AZD2693 in Non-alcoholic Steatohepatitis Patients

Start date: November 6, 2020
Phase: Phase 1
Study type: Interventional

This study is intended to investigate the safety and tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of AZD2693, following subcutaneous (SC) administration of multiple ascending doses in participants with Non-alcoholic Steatohepatitis (NASH) with fibrosis Stage 0 to 3 and who are carriers of the patatin-like phospholipase domain-containing 3 (PNPLA3) 148M risk alleles.

NCT ID: NCT04483518 Completed - Clinical trials for Observe and Describe the Prevalence of Hepatitis D Infection Among HBsAg Positive People

Epidemiological Survey of Hepatitis D Virus Infection in China

Start date: June 3, 2019
Phase:
Study type: Observational

This cross-sectional study will screen out hepatitis D virus-infected patients in HBsAg-positive people. Observe and describe the prevalence of hepatitis D infection among HBsAg positive people. The provinces of China are divided into 5 geographical areas (North, South, East, West and Central) to recruit patients according to the population density of each area. After statistical calculation, the total number of population needed is 3808.