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Healthy clinical trials

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NCT ID: NCT00399737 Terminated - Healthy Clinical Trials

Effects of Peptides Derived From Fermented Milk on Blood Pressure Regulation System in Healthy Volunteers.

Start date: October 2005
Phase: Phase 1
Study type: Interventional

Several milk proteins are precursors of peptides, released during fermentation, which possess various biochemical and physiological properties. Among them, some peptides have been reported to inhibit angiotensin-converting enzyme (ACE) in vitro (an enzyme implicated in blood pressure regulation) and to lower blood pressure (BP). in hypertensive rats and in a small sample of patients with hypertension. One possible mechanism for the BP lowering effect is inhibition of ACE. Prior investigating BP lowering effect of these peptides in a large cohort of hypertensive patients, it is necessary to assess in depth their potency to inhibit ACE in vivo in humans and to compare it to that induced by a well-known ACE inhibitor.

NCT ID: NCT00388219 Terminated - Healthy Clinical Trials

Single Dose Trial Comparing the Plasma Levels of Two Different Analgesic Transdermal Patch Formulations

Start date: October 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether Transtec (R) PRO 70 µg/h and a new buprenorphine patch formulation lead to same plasma levels of buprenorphine after single dose application

NCT ID: NCT00387777 Terminated - Healthy Clinical Trials

Multiple Dose Trial Comparing the Plasma Levels of Two Different Analgesic Transdermal Patch Formulations

Start date: October 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether Transtec(R) PRO 70 µg/h and a new buprenorphine patch formulation lead to same plasma levels of buprenorphine after multiple dose application.

NCT ID: NCT00385892 Terminated - Healthy Clinical Trials

Safety Study of Textile Binder for Abdominal Compression

Start date: August 2005
Phase: N/A
Study type: Interventional

This safety study was carried out to investigate to what extent the use of an abdominal binder influences IAP. The study was designed as a comparative cross-over study measuring bladder pressure.

NCT ID: NCT00315601 Terminated - Healthy Clinical Trials

Intrapulmonary Pharmacokinetics of Antibiotics

Start date: January 2006
Phase: Phase 4
Study type: Interventional

The major objectives of this research are to see how much, and for how long, telithromycin and azithromycin get into the fluids and cells of the lung.

NCT ID: NCT00298857 Terminated - Healthy Clinical Trials

A Pharmacokinetic Study to Compare the Dosing of Valproic Acid in Subjects With Different Body Weights

Start date: March 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the blood levels of valproic acid in subjects with different body weights and to evaluate whether the pharmacokinetic parameters of this drug is altered in the obese population.

NCT ID: NCT00221507 Terminated - Healthy Clinical Trials

Increasing Infant Preventive Health Service Delivery in an Inner City Population

Start date: February 2004
Phase: N/A
Study type: Interventional

The study hypothesis is that case management using patient navigators ("promatoras" in the Latino community) will increase infant immunization rates and use of well child care in an inner city population of low socioeconomic status.

NCT ID: NCT00205140 Terminated - Healthy Clinical Trials

Effect of Pharmacist Initiated Recommendations On Prescribing For Participants In the Senior MEDS Personalized Medication Review

Start date: July 2005
Phase: N/A
Study type: Observational

What are the demographic and medication utilization characteristics of participants in the Senior MEDS personalized medication review compared to other community-dwelling elderly, what is the level of satisfaction with Senior Meds, and does the Senior Meds program lead to changes in the participants' drug regimen?

NCT ID: NCT00167141 Terminated - Healthy Clinical Trials

Contraception in Normal and Subnormal Men

Start date: February 2005
Phase: Phase 2
Study type: Interventional

Volunteers with normal and subnormal semen parameters receive a hormonal male contraceptive in order to investigate whether there are differences between normal and subnormal men in terms of suppressibility, rate of azoospermia and reversibility of suppression of spermatogenesis.

NCT ID: NCT00162786 Terminated - Healthy Clinical Trials

Comparative Effects of Rupatadine 10 mg, Hydroxyzine 50 mg and Placebo on Actual Driving Performance

Start date: May 2005
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to measure and compare the acute effects of rupatadine 10 mg, relative to placebo and hydroxyzine 50 mg as an active control on healthy volunteers’ performance on a standard over-the-road driving test and a car-following test.