Hypertension and edema

Report Year

Trial Code

Trial Title

Clinicaltrials.gov

EudraCTno.

Source

2000

BUX 9501 DK

Bumetanide controlled release capsules in congestive heart failure

N/A

N/A

Summary

Report

Active Substance

bumetanide

LEO Pharma Product

Burinex®

Formulation

tablet & capsule

Trial Phase

2

Population

adults

1999

CE 9401 DK

Efficacy and safety of Centyl® with potassium chloride (bendroflumethiazide) 1.25 mg and 2.5 mg compared to Renitec® (enalapril) 10 mg and Norvasc® (amlodipine) 5 mg in patients with mild to moderate primary

N/A

N/A

Summary

Report

Active Substance

bendroflumethiazide + potassium chloride

LEO Pharma Product

Centryl® K

Formulation

tablet

Trial Phase

3

Population

adults

1999

BU 9202 UK / GP 97

Comparative effects of bumetanide plus captopril in patients with congestive cardiac failure with long-term follow-up for up to two years

N/A

N/A

Summary

Report

Active Substance

bumetanide

LEO Pharma Product

Burinex®

Formulation

tablet

Trial Phase

4

Population

adults

1997

BUFUL NL

A comparative study of the influence of bumetanide and furosemide on the lipidprofile in patients with essential hypertension

N/A

N/A

Summary

Report

Active Substance

bumetanide

LEO Pharma Product

Burinex®

Formulation

tablet

Trial Phase

3

Population

adults

1997

CE 9402 DK

Comparison of Centyl® + KCI 1,25 mg, 2,5 mg(bendroflumethiazid) and Corodil® 10mg (enalapril) in niddm patients with mild to moderate hypertension

N/A

N/A

Summary

Report

Active Substance

bendroflumethiazide + potassium chloride

LEO Pharma Product

Centryl® K & Centryl® K Mite

Formulation

tablet

Trial Phase

3

Population

adults

1992

BX 0309

A comparison of the bioavailability of bumetanide following oral administration as a combined formulation with amiloride and comparison of this with a similar combined formulation of frusemide

N/A

N/A

Summary

Report

Active Substance

bumetanide + amiloride hydrochloride

LEO Pharma Product

N/A

Formulation

tablet

Trial Phase

2

Population

adults

1991

BX 0290

Ingenol mebutate gel, 0.015% repeat use for multiple actinic keratoses on face and scalp

N/A

N/A

Summary

Report

Active Substance

bumetanide + amiloride hydrochloride

LEO Pharma Product

N/A

Formulation

tablet

Trial Phase

2

Population

adults

 

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