A general practice study of timolol/hydrochlorothiazide/amiloride ('Moducren'), a new therapy for hypertension, and the doctor's influence on management

An open study was carried out in general practice to assess the efficacy and tolerance of a timolol (10 mg)/hydrochlorothiazide (25 mg)/amiloride (2.5 mg) preparation in 558 hypertensive patients previously receiving multi-dose antihypertensive therapy, and to determine whether the results were infl...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Interim guidelines for the control of infections with Vero cytotoxin producing Escherichia coli (VTEC). Subcommittee of the PHLS Working Group on Vero cytotoxin producing Escherichia coli (VTEC). - 1995. - 3(1983), 5 vom: 01., Seite 294-9
1. Verfasser: Parry, E E (VerfasserIn)
Weitere Verfasser: Arr, S, Tait, D
Format: Aufsatz
Sprache:English
Veröffentlicht: 1983
Zugriff auf das übergeordnete Werk:Interim guidelines for the control of infections with Vero cytotoxin producing Escherichia coli (VTEC). Subcommittee of the PHLS Working Group on Vero cytotoxin producing Escherichia coli (VTEC)
Schlagworte:Clinical Trial Journal Article Randomized Controlled Trial Drug Combinations Propanolamines Pyrazines Hydrochlorothiazide 0J48LPH2TH moducrin 73788-01-9 mehr... Amiloride 7DZO8EB0Z3 Timolol 817W3C6175
Beschreibung
Zusammenfassung:An open study was carried out in general practice to assess the efficacy and tolerance of a timolol (10 mg)/hydrochlorothiazide (25 mg)/amiloride (2.5 mg) preparation in 558 hypertensive patients previously receiving multi-dose antihypertensive therapy, and to determine whether the results were influenced by the manner in which the doctor conducted this change in therapy. Patients received 1 or, if necessary, 2 tablets once daily over a period of 12 weeks and were randomly allocated on entry to one of two groups. One group was given a full explanation for the change in therapy, the other group was simply told that treatment was to be changed. The results showed that the change in treatment led to a significant reduction in blood pressure in both groups, at a dosage of 1 tablet daily in over half the patients, and the majority (88%) preferred the new form of treatment. Patient acceptance was good and the number of reports of adverse symptoms decreased during the study period. There was no significant difference in any of the results between the two groups
Beschreibung:Date Completed 10.06.1983
Date Revised 21.11.2013
published: Print
Citation Status MEDLINE