The objective of this study was to compare, at equal blood pressure (BP) reduction, the effect of two different combinations on metabolic control and albuminuria in type 2 diabetic hypertensive patients with albuminuria. This was a prospective, randomised, double-blind, parallel, controlled trial carried out in 11 Spanish hospitals. A total of 103 type 2 diabetic patients with stable albuminuria and BP not controlled on monotherapy were randomised of which 93 finished the study. After a 4-week single-blind placebo period, patients were randomised to verapamil SR/trandolapril 180/2 mg (VT) or to enalapril/hydroclorothiazide 20/12.5 mg (EH). Treatment duration was 6 months. The main outcome measures were changes in BP, 24-h albuminuria, blood glucose and glycated haemoglobin. Overall BP was significantly reduced from 157.3+/-12.0/98.3+/-6.4 mm Hg to 140.5+/-14.5/86.1+/-8.2 mm Hg (P<0.001) and albuminuria significantly decreased from 508.6 +/- 693.8 mg/24 h to 253.4 +/- 517.2 mg/24 h (P<0.001), both without significant differences between treatments. Glycated haemoglobin was not modified on VT: baseline, 5.91+/-1.43%; end of treatment, 5.94+/-1.62%, but increased on EH: baseline, 5.96+/-1.25%; final, 6.41+/-1.51%, (ANOVA interaction P=0.040). At the end of the study, a blood glucose <126 mg/dL was attained in 72.7% of the VT group-improving in 29.5% and worsening in 6.8% of patients (P=0.021)-and in 50% of the EH group, 13.6% of patients improved and 11.4% worsened (P=1.000). There were no changes in body weight, serum creatinine, uric acid, potassium, cholesterol, tryglicerides and serum albumin. In hypertensive type 2 diabetic patients not controlled on monotherapy, both treatments similarly reduced albuminuria. The combination verapamil/trandolapril seems to allow a better metabolic control than enalapril/hydroclorothiazide.