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Healthy Adults clinical trials

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NCT ID: NCT05330000 Completed - Healthy Adults Clinical Trials

Comparative Study on Tolerance and Pharmacokinetics of Voriconazole for Injection in Healthy Subjects

Start date: May 22, 2020
Phase: Phase 1
Study type: Interventional

A single intravenous drip of voriconazole for injection developed by Qilu Pharmaceutical (Hainan) Co., Ltd. and the original product "vfend" was given to healthy subjects , The pharmacokinetic differences and tolerance of the two preparations were evaluated at the doses of 4mg / kg and 6mg / kg.

NCT ID: NCT05326776 Completed - Healthy Adults Clinical Trials

Peripheral Oxytocin and Touch

POPP
Start date: April 5, 2023
Phase: Phase 2
Study type: Interventional

Research shows that slow gentle skin stroking can activate special sensory nerves in the skin that elicit relaxing effects on the body and mind, similar to the effects of the hormone oxytocin. Studies also suggest that gentle stroking may even release oxytocin in the skin. However, we do not know what oxytocin does in the skin and how it affects nerves that send pleasant touch or pain signals to the brain. The proposed study will determine how individuals perceive gentle stroking and experimental pain before and after a skin injection of oxytocin compared to a placebo injection.

NCT ID: NCT05255276 Completed - Healthy Adults Clinical Trials

PK Study to Assess Drug-drug Interaction Between Sitravatinib and a P-gp Inducer and an Inhibitor.

Start date: February 2, 2022
Phase: Phase 1
Study type: Interventional

A Phase 1 Open-label, Two-cohort, One-sequence Crossover Study to Investigate the Effect of P glycoprotein Inhibitor (Itraconazole) and Inducer (Rifampin) on the Pharmacokinetics, Safety, and Tolerability of Sitravatinib in Healthy Subjects.

NCT ID: NCT05210634 Completed - Healthy Adults Clinical Trials

Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of CHI-915 in Healthy Participants

Start date: January 11, 2022
Phase: Phase 1
Study type: Interventional

This is a two-phase, randomized, double-blind, placebo-controlled, within-participant crossover study to assess the safety, tolerability, PK, and PD of five oral doses of CHI-915 versus placebo in healthy adult participants ages 18-55 years.

NCT ID: NCT05141903 Completed - Healthy Adults Clinical Trials

Dietary Supplement With and Without a Probiotic and/or Antibiotic

Start date: September 21, 2021
Phase:
Study type: Observational

Complex oligosaccharides can alter the gut microbiome by aiding in the growth of certain organisms, and possibly, inhibiting others. The synergy with a probiotic may enhance gastrointestinal colonization.

NCT ID: NCT05093205 Completed - Healthy Adults Clinical Trials

STUDY TO EVALUATE THE EFFECT OF PF-06882961 ON SINGLE DOSE ATORVASTATIN, MEDAZOLAM AND ORALCONTRACEPTIVE PHARMACOKINETICS IN HEALTHY ADULT PARTICIPANTS

Start date: October 25, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study is to characterize the effect of PF-06882961, administered at 2 steady-state dose levels, on the PK of single doses of atorvastatin (20 mg) or midazolam (5 mg), administered separately, in healthy adult male and female participants (Part A), or an OC in healthy PM female participants (Part B).

NCT ID: NCT05078346 Completed - Healthy Adults Clinical Trials

Immune Fitness Prediction

Start date: June 2, 2021
Phase:
Study type: Observational

The overall objective of the study is to determine whether self-rated, perceived immune fitness (using questionnaire) is associated with biological assessment of immune fitness (immune signatures in the blood).

NCT ID: NCT04994743 Completed - Healthy Adults Clinical Trials

Safety, Tolerability, and Pharmacokinetic Study of CORT113176 in Healthy Participants

Start date: July 13, 2021
Phase: Phase 1
Study type: Interventional

This is a safety, tolerability, and pharmacokinetic study in 2 cohorts of healthy male participants with an option for an additional cohort. Cohorts 1 and 2 will receive once daily by mouth CORT113176 150 mg and 300 mg, respectively, for 14 days under fed conditions. Progression from Cohort 1 to Cohort 2 will be done based on the safety and tolerability outcome in Cohort 1 and after Cohort 1 has received the study drug for at least 7 days. The optional Cohort 3 may receive a higher dose that will not exceed CORT113176 450 mg once daily by mouth for 14 days under fed conditions. The progression from Cohort 2 to the optional cohort (Cohort 3) will be based on the same precautions as with the progression from Cohort 1 to Cohort 2. Each participant will undergo safety evaluations. Pharmacokinetics of CORT113176 will be assessed in plasma and cerebrospinal fluid (CSF) samples. Pharmacodynamic assessments will include the measurement of serum cortisol.

NCT ID: NCT04935112 Completed - Healthy Adults Clinical Trials

A Study to Explore the Effect of Acid-reducing Agents

Start date: July 7, 2021
Phase: Phase 1
Study type: Interventional

A Phase 1 Study of the Effect of Acid-reducing Agents on the Pharmacokinetics of a Single Oral Dose of Sitravatinib in Healthy Adult Subjects. The study is a single-center, open-label, 2-period, 2-treatment, fixed-sequence crossover, parallel-group study.

NCT ID: NCT04910932 Completed - Healthy Adults Clinical Trials

Effects of Breathing Exercises on Fear of COVID-19, Anxiety, Sleep and Quality of Life During the COVID-19 Pandemic

Start date: June 10, 2021
Phase: N/A
Study type: Interventional

It has been reported that in the first stages of the pandemic, a significant portion of the general population experienced psychological problems such as anxiety, depression and post-traumatic disorders. These problems persist today. A balanced diet, physical activity participation and relaxation techniques are recommended for preventing such problems. In studies conducted before the pandemic, it is reported that breathing exercises have positive effects on anxiety, sleep and quality of life in both patients and healthy individuals. Aim of this study is to investigate the effects of breathing exercises applied via teleconference on fear of COVID-19, anxiety, sleep and quality of life in healthy adult population.