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Active clinical trials for "Malnutrition"

Results 491-500 of 1358

Bioequivalence Study of Ropinirole Hydrochloride ER Tablets 2 mg Under Fed Condition

Healthy

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

Completed26 enrollment criteria

Is Multifactorial Nutritional Treatment for Undernutrition in Older Adults in Primary Care Cost-effective?...

Frail Older Adults

The hypothesis is that there is a profit potential by implementing a multifactorial nutritional intervention among frail elderly since this will result in an improved nutritional status, functional capacity and improved quality of life.

Completed2 enrollment criteria

Bioequivalence Study of Metformin Hydrochloride Extended-Release Tablets USP 750 mg Under Fed Condition...

Fasting

The study was a randomized, open label, two-treatment, two-period, two-sequence, single dose, crossover, oral bioequivalence study in normal, healthy adult human subjects under fed condition.

Completed30 enrollment criteria

Bioequivalence Study of Lamotrigine Extended-Release Tablets 200mg 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

A Prospective Study Frailty for Esophagectomy and Lung Resection in Thoracic Surgery

ThoracicThoracic Neoplasm7 more

The purpose of this study is to develop an all-encompassing frailty model using laboratory and functional studies. A frailty model will help us determine prior to surgery who will require rehabilitation and skilled nursing needs beyond discharge. This model will also help us determine who will likely be readmitted and why they will be readmitted. Understanding these things can help us prevent some of them from occurring in the future.

Active2 enrollment criteria

Comparison of an Alternative Therapeutic Food for the International Food Aid Market to a Standard...

Malnutrition

In this clinical non-inferiority trial, two foods will be compared for the treatment of SAM, testing the hypothesis that the difference in recovery rates and growth between the two test groups will be no greater than 5 percent.

Completed7 enrollment criteria

Bioequivalence Study of Tetrabenazine Tablets 25 mg Under Fed Conditions

Healthy

This is an open-label, randomized, four-period, two-treatment, two-sequence, balanced, single dose, crossover, oral bioequivalence study in healthy, adult, human subjects under fed conditions.

Completed29 enrollment criteria

Integrated Treatment Protocol for Acute Malnutrition: A Non Inferiority Trial in Burkina Faso

Global Acute Malnutrition (GAM)

MUAC only is a pilot trial external control carried out between January 2017 and December 2017 in the Yako district (northern region), Burkina Faso. The objective of this study is to evaluate an integrated protocol for acute malnourished children without medical complication. The hypotheses of the integrated protocol include : A global treatment of acute malnutrition (moderate and severe) with a single treatment (RUTF) would improve the functioning of the program through early identification of acutely malnourished children, while achieving a better coverage and using a single supply chain. A gradual reduction of RUTF dosage according to a child's MUAC status could significantly increase the number of children on treatment without increasing overall RUTF quantity while maintaining similar recovery rates.

Completed9 enrollment criteria

Treatment of High-Risk Moderate Acute Malnutrition Using Expanded Admission Criteria

Malnutrition

This project explores whether children have better growth and cognitive development when the clinic identifies "higher risk" MAM children and support them either with the same treatment as SAM children or with the recommended practice: nutrition counseling.

Completed5 enrollment criteria

Bioequivalence Study of Oseltamivir Phosphate and TAMIFLU Under Fed Condition in Healthy Volunteers...

Bioequivalence

This study is to evaluate the bioequivalence of Oseltamivir Phosphate Capsules 75 mg versus TAMIFLU 75 mg capsules administered as 75 mg capsules in healthy volunteers under Fed condition.

Completed32 enrollment criteria
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