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NCT ID: NCT05060367 Completed - Mineral Absorption Clinical Trials

Pharmacokinetic Analysis of Nutrient Absorption From a Novel Liposomal Multivitamin/Mineral Formulation

Start date: September 16, 2021
Phase: N/A
Study type: Interventional

This project is a randomized crossover trial examining the pharmacokinetic profiles of standard and liposomal multivitamin/mineral (MVM) formulations in healthy adults. Each participant will complete two research visits, which will be identical except for which MVM product is consumed. At each visit, participants will report to the laboratory after an overnight fast. After a baseline blood sample is collected, the MVM product will be consumed alongside a standardized breakfast. At 2-, 4-, and 6-hours post-ingestion, additional blood samples will be collected. Concentrations of representative minerals will be analyzed to determine whether differential nutrient absorption is observed with the liposomal MVM as compared to the standard MVM product. The results of this study will provide information about a novel liposomal MVM formulation and will inform future research and commercial applications of this technology.

NCT ID: NCT05060354 Completed - Healthy Clinical Trials

COVID-19 Vaccine Response in Treated MS Patients

Start date: June 1, 2021
Phase:
Study type: Observational

The primary goal of this study is to assess the impact of the two major disease modifying therapy (DMT) classes (B cell therapies and S1P modulators) on humoral and cell-mediated immunity to SARS- CoV-2 vaccination compared to non-MS controls. We have chosen to compare DMT-treated MS patients to non-MS controls because the pivotal vaccine studies were conducted in non-MS healthy control groups in which there is significant clinical data and validated assays for antibody responses.

NCT ID: NCT05060328 Completed - Clinical trials for Malignant Solid Neoplasm

Use of Google Translate to Enhance Patient Pain and Nausea Assessment and Satisfaction After General Anesthesia

Start date: June 22, 2021
Phase:
Study type: Observational

This study investigates the use of Google Translate "Conversation Mode" translation service to improve communication about pain and nausea with Spanish-speaking patients who are recovering after surgery. The Google Translate "Conversation Mode" translation application is designed to provide translation from one language to another and used to allow the nurse or study doctor to communicate with patients in Spanish by asking pre-prepared questions through an electronic device such as an iPad or iPhone. Google Translate "Conversation Mode" may facilitate assessment of pain and nausea after surgery in Spanish speaking patients.

NCT ID: NCT05060237 Completed - Actinic Keratosis Clinical Trials

Study to Evaluate Safety and Tolerability of BF-200 ALA (Ameluz®) for Photodynamic Therapy in the Treatment of the Expanded Field of Actinic Keratosis on Face and Scalp

Start date: December 1, 2021
Phase: Phase 1
Study type: Interventional

The aim of the study is to evaluate the safety and tolerability of PDT for treatment of mild to severe actinic keratosis on the face and scalp in the expanded treatment field using 3 tubes of BF-200 ALA 10% gel (Ameluz®) in conjunction with the BF-RhodoLED® XL PDT lamp.

NCT ID: NCT05059977 Completed - Healthy Volunteers Clinical Trials

A Study of TAK-881 in Healthy Adults

Start date: October 12, 2021
Phase: Phase 1
Study type: Interventional

The main aims of this study are to check for side effects from TAK-881 in healthy adults and to learn how much TAK-881 they can receive without getting side effects from it. During the study, participants will receive one infusion of TAK-881 under the skin (subcutaneous infusion) on Day 1 at a lower dose level followed by participants receiving one infusion of higher dose levels with ongoing safety monitored by the doctor to ensure optimal tolerability and safety. Participants will stay in the clinic for 4 days and will come back after 4 weeks. A follow up visit will take place 12 weeks after the TAK-881 infusion.

NCT ID: NCT05059730 Completed - Hypothermia Clinical Trials

Comparison of Bi-environmental Conditions During Occupational Related Activity

COBRA
Start date: April 2, 2021
Phase: N/A
Study type: Interventional

BHSAI is developing a computational system that provides early alerts of a rise and fall in core body temperature to help reduce the risk of thermal injury in the field and during training. The goal of the body temperature alerting system is to use it during rest, exercise in the heat and cold. Therefore, the primary purpose of this investigation is to validate a body temperature alerting system using physiological responses that occur during rest, exercise in the heat and cold. Multiple cold ambient temperatures will be validated.

NCT ID: NCT05059691 Completed - Lung Carcinoma Clinical Trials

Three-Dimensional Fluoroscopic Guidance During Transbronchial Cryobiopsy

Start date: March 30, 2021
Phase:
Study type: Observational

This study assesses the effectiveness of transbronchial cryobiopsy guided by 3-dimensional fluoroscopy. Transbronchial cryobiopsy is a procedure to collect lung tissue. The main side effect seen after a transbronchial cryobiopsy is pneumothorax (air leaking out of the lung, which may cause a completely or partially collapsed lung). The standard imaging scans used during this procedure are 2-dimensional (like a photo), which can make it difficult for the doctor to know exactly where the biopsy tool is during the procedure. If the exact location of the device is not clear, a patient can be at a higher risk of pneumothorax. Using a 3-dimensional imaging technique may help to decrease the risk of pneumothorax during transbronchial cryobiopsy.

NCT ID: NCT05059600 Completed - Clinical trials for Postpartum Depression

A Study To Assess The Safe-Use Conditions For Administration of ZULRESSO® in a Home Setting

Start date: October 8, 2021
Phase: Phase 4
Study type: Interventional

The primary purpose of this study was to evaluate whether the safe-use conditions for administration of brexanolone (ZULRESSO®) can be implemented in a home setting.

NCT ID: NCT05059366 Completed - Ventilator Lung Clinical Trials

Manual Ventilation Efficacy With MVG Device

Start date: August 11, 2021
Phase: N/A
Study type: Interventional

The purpose of this research is to investigate the efficacy of the newly designed ventilation grip device (MVG device).

NCT ID: NCT05059301 Completed - Clinical trials for Respiratory Syncytial Virus Infections

A Study of 3 Lots of an Investigational Vaccine Against Respiratory Syncytial Virus (RSV) in Adults Aged 60 Years and Above

Start date: October 1, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the lot-to-lot consistency in terms of immunogenicity and evaluate the safety and reactogenicity of 3 lots of the RSVPreF3 OA investigational vaccine administered as a single dose in adults ≥ 60 years of age (YOA).