Literature DB >> 6499895

Crossover comparison of moxonidine and clonidine in mild to moderate hypertension.

V Plänitz.   

Abstract

The antihypertensive effect of moxonidine X HCl X H2O (MOX) was compared with that of clonidine X HCl (CLON) in a randomized double-blind crossover study in 20 hypertensive outpatients (BP range 154-178/96-108 mmHg). After 2 weeks without antihypertensive medication, either MOX 0.2 mg daily or CLON 0.2 mg daily was given and the dose was titrated until the diastolic blood pressure fell below 90 mmHg. The first treatment period was continued for 2 weeks and, after crossover without a wash-out period, it was followed by the second treatment for a further 2 weeks. Within the first 4 days of administration 0.2-0.4 mg of either agent caused a significant decrease in BP (p less than 0.001) from a mean of 166/100 mmHg to 149/86 mmHg after CLON (approx. -10/-14%), and 163/99 mmHg to 146/84 mmHg after MOX (approx. -10/-15%). No significant difference in the fall in BP or pulse rate was detected between the two drugs. In the mean daily dose of 0.3 mg both drugs showed the same antihypertensive activity, but on CLON a higher incidence of side effects (p = 0.003) was noted, and after discontinuation of therapy a more rapid rise in BP (systolic BP p less than 0.01, diastolic BP p less than 0.02) was found. 17 patients on CLON complained of side effects, especially tiredness and dry mouth, whilst only 6 patients on MOX were affected (p = 0.003).

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Year:  1984        PMID: 6499895     DOI: 10.1007/bf00544037

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  18 in total

1.  Antihypertensive effect of clonidine. Its use alone and in combination with hydrochlorothiazide and guanethidine in the treatment of hypertension.

Authors:  B K Yeh; A Nantel; L I Goldberg
Journal:  Arch Intern Med       Date:  1971-02

2.  The antihypertensive effects of an imidazoline compound.

Authors:  M Davidov; N Kakaviatos; F A Finnerty
Journal:  Clin Pharmacol Ther       Date:  1967 Nov-Dec       Impact factor: 6.875

3.  Blood pressure crisis following withdrawal of clonidine (Catapres, Catapresan), with special reference to arterial and urinary catecholamine levels, and suggestions for acute management.

Authors:  L Hansson; S N Hunyor; S Julius; S W Hoobler
Journal:  Am Heart J       Date:  1973-05       Impact factor: 4.749

4.  Studies on catecholamines, renin and aldosterone following Catapresan (2-(2,6-dichlor-phenylamine)-2-imidazoline hydrochloride) in hypertensive patients.

Authors:  B Hökfelt; H Hedeland; J F Dymling
Journal:  Eur J Pharmacol       Date:  1970       Impact factor: 4.432

5.  Clinical observations on a new antihypertensive drug, 2-(2,6-dichlorphenylamine)-2-imidazoline hydrochloride.

Authors:  G Smet; S W Hoobler; S Sanbar; S Julis
Journal:  Am Heart J       Date:  1969-04       Impact factor: 4.749

6.  Properties of catapres, a new hypotensive drug: a preliminary report.

Authors:  J Ng; D D McGrgor; K M Taylor; H Smirk
Journal:  N Z Med J       Date:  1967-12

7.  Clonidine: an introduction.

Authors:  J A Wilber
Journal:  J Cardiovasc Pharmacol       Date:  1980       Impact factor: 3.105

8.  Pharmacokinetic and concentration-effect relationships of clonidine in essential hypertension.

Authors:  L M Wing; J L Reid; D S Davies; E A Neill; P Tippett; C T Dollery
Journal:  Eur J Clin Pharmacol       Date:  1977-12-28       Impact factor: 2.953

9.  [Patient cooperation in hypertensive therapy (author's transl)].

Authors:  H Holzgreve
Journal:  MMW Munch Med Wochenschr       Date:  1980-02-22

10.  Clonidine withdrawal in hypertension. Changes in blood-pressure and plasma and urinary noradrenaline.

Authors:  J L Reid; L M Wing; H J Dargie; C A Hamilton; D S Davies; C T Dollery
Journal:  Lancet       Date:  1977-06-04       Impact factor: 79.321

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  21 in total

Review 1.  Centrally acting antihypertensive drugs: re-emergence of sympathetic inhibition in the treatment of hypertension.

Authors:  C R Benedict
Journal:  Curr Hypertens Rep       Date:  1999-08       Impact factor: 5.369

2.  Central nervous system effects of moxonidine experimental sustained release formulation in patients with mild to moderate essential hypertension.

Authors:  Michiel J B Kemme; Jeroen P vd Post; Rik C Schoemaker; Matthias Straub; Adam F Cohen; Joop M A van Gerven
Journal:  Br J Clin Pharmacol       Date:  2003-06       Impact factor: 4.335

Review 3.  Drugs acting on imidazoline receptors: a review of their pharmacology, their use in blood pressure control and their potential interest in cardioprotection.

Authors:  P Bousquet; J Feldman
Journal:  Drugs       Date:  1999-11       Impact factor: 9.546

4.  A comparison of the haemodynamic and behavioural effects of moxonidine and clonidine in normotensive subjects.

Authors:  G J Macphee; C A Howie; H L Elliott; J L Reid
Journal:  Br J Clin Pharmacol       Date:  1992-03       Impact factor: 4.335

Review 5.  The I1-imidazoline receptor: from binding site to therapeutic target in cardiovascular disease.

Authors:  P Ernsberger; J E Friedman; R J Koletsky
Journal:  J Hypertens Suppl       Date:  1997-01

6.  The influence of renal function on clinical pharmacokinetics of moxonidine.

Authors:  W Kirch; H J Hutt; V Plänitz
Journal:  Clin Pharmacokinet       Date:  1988-10       Impact factor: 6.447

Review 7.  Medication management on sick days.

Authors:  Tom N Lea-Henry; Jonathan Baird-Gunning; Elizabeth Petzel; Darren M Roberts
Journal:  Aust Prescr       Date:  2017-10-03

8.  A Prospective Real World Experience of Moxonidine Use in Indian Hypertensive Patients-Prescription beyond Current Guidelines.

Authors:  Suresh V Sagarad; Sudha Biradar-Kerure; Ramakrishna Mr; Chaitanya Kumar S; S S Reddy
Journal:  J Clin Diagn Res       Date:  2013-10-05

9.  Renal imidazoline preferring sites and solute excretion in the rat.

Authors:  D R Allan; S B Penner; D D Smyth
Journal:  Br J Pharmacol       Date:  1993-04       Impact factor: 8.739

Review 10.  Moxonidine. A review of its pharmacology, and therapeutic use in essential hypertension.

Authors:  P Chrisp; D Faulds
Journal:  Drugs       Date:  1992-12       Impact factor: 9.546

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