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Active clinical trials for "Malnutrition"

Results 431-440 of 1358

Bioequivalence Study of Risperidone Tablet 1 mg Under Fed Condition

Fed

This is a randomized, open Label, balanced, two-treatment, two-period, two-sequence, single dose, crossover pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fed condition in normal, healthy, adult human subjects.

Completed32 enrollment criteria

Bioequivalence Study of Lamotrigine Tablets 25 mg (2 x 25 mg Tablets) Under Fed Condition

Fed

This is an open Label, randomized, two-period, two-treatment, two-sequence, crossover, balanced, single dose pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fed condition in healthy adult human subjects.

Completed39 enrollment criteria

Crossover Bioequivalence Study of Irbesartan 300 mg Tablets Under Fed Conditions

Hypertension

The objective of this study was to prove the bioequivalence of Roxane Laboratories' Irbesartan 300 mg Tablets under fed conditions.

Completed19 enrollment criteria

Bioequivalence Study of Montelukast Sodium Tablets 10mg Under Fed Condition

Healthy

This is an open label, randomised, balanced, two-treatment, two-period, two-sequence, single dose, crossover, oral bioequivalence study.

Completed27 enrollment criteria

Bioequivalence Study of Etodolac Tablet USP 500 mg Under Fed Condition

Fed

This is a open Label, balanced, randomized, single dose, two-treatment, two-sequence, two-period, crossover pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fed condition in healthy, adult human subjects.

Completed33 enrollment criteria

Women First: Preconception Maternal Nutrition

Maternal MalnutritionGrowth Failure3 more

Multi-country three-arm, individually randomized, non-masked, controlled trial to ascertain the benefits of ensuring optimal maternal nutrition before conception and providing an evidence base for programmatic priority directed to minimizing the risk of malnutrition in all females of reproductive age.

Completed4 enrollment criteria

Bioequivalence Study for Donepezil Hydrochloride Tablets 10 mg Under Fed Condition

Healthy

This is an open label, balanced, randomized, two-treatment, two-period, two sequence, single dose, crossover, oral bioequivalence study.

Completed25 enrollment criteria

Crossover Bioequivalence Study of Quetiapine Fumarate 25 mg Tablets Under Fed Conditions

Bipolar I Disorder

The objective of this study was to prove the bioequivalence of Roxane Laboratories' Quetiapine Fumarate 25 mg Tablet under fed conditions.

Completed4 enrollment criteria

Bioequivalence Study of Ondansetron Tablets USP 8 mg Under Fed Condition

Fed

This is a randomized, open Label, balanced, two-treatment, two-period, two-sequence, single dose, cross over pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fed condition in normal, healthy, adult, human subjects.

Completed31 enrollment criteria

Feeding the Patient at Nutritional Risk: Does the Clinical Outcome Improve?

Malnutrition

The aim of the present study is to take stronger action in solving the problems of malnutrition in the hospital setting and in the first two months after patient's discharge. The main objective is to evaluate the clinical benefit (eg. QoL, body composition and body function) of nutritional intervention (nutritional therapy) in a sample of patients at nutritional risk according to the NRS 2002.

Completed13 enrollment criteria
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