pathology | treatment | patient | Demonstrated benefit and harm | k | | | |
---|
diabetes type 2 | gliclazide | not classified | versus No demonstrated result for efficacy | 3 trials | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
Khanolkar, 2008 | gliclazide vs rosiglitazone (add on MET) | | | | Ristic, 2006 | gliclazide vs nateglinide (add on MET) | | | | Matthews, 2005 | gliclazide vs pioglitazone (add on MET) | | | |
Trial | Treatments | Patients | Method |
---|
Khanolkar, 2008 | metformin and gliclazide (n=-9) vs. metformin and rosiglitazone (n=-9) | | Sample size: -9/-9 Primary endpoint: FU duration: 24 weeks | Ristic, 2006 | gliclazide plus metformin (n=-9) vs. nateglinide plus metformin (n=-9) | | double-blind Sample size: -9/-9 Primary endpoint: FU duration: 52 weeks | Matthews, 2005 | gliclazide 80 mg o.d. (titrated up to 320 mg (n=313) vs. pioglitazone 15 mg o.d. (titrated up to 45 mg (n=317) | Patients with poorly controlled type 2 diabetes | double-blind Sample size: 313/317 Primary endpoint: FU duration: 52 weeks |
|
diabetes type 2 | glimepiride | not classified | versus No demonstrated result for efficacy | 1 trial | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
Charpentier, 2001 | glimepiride monotherapy vs metformin | | | |
Trial | Treatments | Patients | Method |
---|
Charpentier, 2001 | glimepiride monotherapy (n=-9) vs. metformin monotherapy (n=-9) | Type 2 diabetic patients aged 35-70 years inadequately controlled by metformin monotherapy 2550 mg daily for at least 4 weeks | double-blind Sample size: -9/-9 Primary endpoint: FU duration: 20 weeks |
|
diabetes type 2 | glimeripide | not classified | versus No demonstrated result for efficacy | 1 trial | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
LEAD-2 (Nauck) Sulf vs pbo, 2009 | glimepiride vs placebo (add on MET) | | | |
Trial | Treatments | Patients | Method |
---|
LEAD-2 (Nauck) Sulf vs pbo, 2009 | glimepiride (4 mg once daily). (n=-9) vs. placebo (n=-9) | subjects previously treated with oral antidiabetes (OAD) therapy | double-blind Sample size: -9/-9 Primary endpoint: FU duration: 26 weeks |
|
diabetes type 2 | glimeripide | not classified | versus placebo No demonstrated result for efficacy | 8 trials | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
| T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | Charpentier, 2001 | glimepiride vs placebo (add on MET) | | | CV death 1.00 [0.38; 2.62] All-cause mortality 1.00 [0.38; 2.62] Stroke 1.00 [0.38; 2.62] Myocardial infarction 1.00 [0.38; 2.62] | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | |
Trial | Treatments | Patients | Method |
---|
Study 201 (Goldberg), 1996 | glimepiride, 1, 4, or 8 mg once daily (n=304) vs. placebo (n=0) | patients with NIDDM | double-blind Parallel groups Sample size: 304/0 Primary endpoint: FU duration: 14 weeks | Schade, 1998 | glimepiride at individually determined optimal dose (1-8 mg of glimepiride) for 10+12 weeks (n=123) vs. placebo (n=126) | patients with type 2 diabetes mellitus for whom diet therapy is unsuccessful | double-blind Parallel groups Sample size: 123/126 Primary endpoint: FU duration: | Rosenstock, 1996 | glimepiride 8 mg q.d., 4 mg b.i.d., 16 mg q.d., or 8 mg b.i.d (n=416) vs. placebo (n=0) | previously treated NIDDM patients | double-blind Parallel groups Sample size: 416/0 Primary endpoint: FU duration: 14 weeks | Luis Bautista, 2003 | glimepiride with titration to 2 mg and 4 mg for FPG levels >120 mg/dL (n=-9) vs. placebo (n=-9) | Mexican American Patients with type 2 diabetes mellitus | double-blind Parallel groups Sample size: -9/-9 Primary endpoint: change in HbA(1c) FU duration: 14 weeks | Charpentier, 2001 | metformin and glimepiride (n=-9) vs. metformin (n=-9) metformin, glimepiride or metformin and glimepiride | Type 2 diabetic patients aged 35-70 years inadequately controlled by metformin monotherapy 2550 mg daily | double-blind Sample size: -9/-9 Primary endpoint: FU duration: | Kaneko, 1993 | glimepiride 0.25mg od, 0.5mg od (n=62) vs. placebo (n=31) | | Sample size: 62/31 Primary endpoint: FU duration: | Study 202 | glimepiride 1-8mg od (n=122) vs. placebo (n=125) | | Sample size: 122/125 Primary endpoint: FU duration: | Riddle, 1994 | Glimepiride (16 mg/day) plus insulin (n=72) vs. insulin
plus placebo (n=73) | obese
patients with type 2 diabetes insufficiently controlled
by full dosages of sulphonylureas (glimepiride titrated up to 8mg twice daily and with laboratory-monitored FPG of 10 to 16
mmol/L (180 to 300 mg/dl)) | Sample size: 72/73 Primary endpoint: FU duration: |
|
diabetes type 2 | glimeripide | not classified | versus gliclazide No demonstrated result for efficacy | 1 trial | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
| T1 vs T0 | | | |
Trial | Treatments | Patients | Method |
---|
Charpentier (301F) | glimepiride 1-4mg od (n=96) vs. gliclazide 80-320 mg/day (od or bid) (n=107) | | Sample size: 96/107 Primary endpoint: FU duration: |
|
diabetes type 2 | glimeripide | not classified | versus Sulfonylurea No demonstrated result for efficacy | 6 trials | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
| T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | |
Trial | Treatments | Patients | Method |
---|
Draeger, 1996 | glimepiride 1 mg daily (n=524) vs. 2.5 mg glibenclamide (n=520) | type 2 diabetic patients stabilised on glibenclamide | double-blind Parallel groups Sample size: 524/520 Primary endpoint: not unique FU duration: | Dills, 1996 | glimepiride 1-16mg od (n=289) vs. non-micronized glyburide 1.25-20mg od (n=288) | patients with non-insulin dependent diabetes | double-blind Parallel groups Sample size: 289/288 Primary endpoint: FU duration: | Inukai, 2005 | glimepiride (n=172) vs. gliclazide or glibenclamide (n=0) | Japanese type 2 diabetic patients (HbA1C > or = 7.0%), maintained on a conventional SU | open Parallel groups Sample size: 172/0 Primary endpoint: FU duration: 6 months | Protocol 311 | glimepiride 1-8mg od (n=427) vs. glibenclamide 1.75-14 mg/day
(od or bid) (n=425) | | Sample size: 427/425 Primary endpoint: FU duration: | Clark (301), 1997 | glimepiride 1-16 mg/day (od or bid) (n=444) vs. glipizide 2.5-40 mg/day (od or bid) (n=208) | | Sample size: 444/208 Primary endpoint: FU duration: | Sonnenberg, 1997 | glimepirid e6mg od (n=50) vs. glimepiride 3mg bid (n=48) | | Cross over Sample size: 50/48 Primary endpoint: FU duration: |
|
diabetes type 2 | glipizide | not classified | versus No demonstrated result for efficacy | 8 trials | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
Nauck, 2007 | glipizide vs sitagliptin (add on MET) | | | | Feinglos, 2005 | glipizide GITS vs placebo (add on MET) | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | |
Trial | Treatments | Patients | Method |
---|
Nauck, 2007 | glipizide (n=-9) vs. sitagliptin (n=-9) | | Sample size: -9/-9 Primary endpoint: FU duration: 52 weeks | Feinglos, 2005 | 2.5 mg glipizide GITS (n=61) vs. placebo (n=61) | type 2 diabetes inadequately controlled (A1c 7-8.5%) on metformin (> or =1000 mg/day for > or =3 months) | double-blind Sample size: 61/61 Primary endpoint: FU duration: 16 weeks | Rosenstock, 1993 | glipizide, 2.5 or 5 mg/day (n=139) vs. glyburide, 1.25 or 2.5 mg/day (n=0) | elderly patients with NIDDM that was controlled for at least 3 months with oral sulfonylurea therapy | open Parallel groups Sample size: 139/0 Primary endpoint: FU duration: 4 months | Birkeland, 1994 | glipizide (n=-9) vs. glyburide (n=-9) | NIDDM patients | Sample size: -9/-9 Primary endpoint: FU duration: | Birkeland, 1994 | glipizide (n=-9) vs. glyburide (n=-9) | NIDDM patients | double-blind Parallel groups Sample size: -9/-9 Primary endpoint: FU duration: 15 months | Simonson, 1997 | once-daily doses of 5, 20, 40, or 60 mg glipizide GITS (n=-9) vs. placebo (n=-9) | NIDDM patients | double-blind Parallel groups Sample size: -9/-9 Primary endpoint: FU duration: 4+8 weeks | Testa, 1998 | 5 to 20 mg of glipizide gastrointestinal therapeutic system (GITS) (n=377) vs. placebo (n=192) | patients with type 2 diabetes mellitus | Parallel groups Sample size: 377/192 Primary endpoint: FU duration: 12 weeks | Goldstein | glipizide/metformin 5/500 mg tablets (n=-9) vs. metformin 500-mg (n=-9) glipizide 30-mg, metformin 500-mg, or glipizide/metformin 5/500 mg | patients with type 2 DM that is uncontrolled by at least half the maximum labeled daily dose of a sulfonylurea | open Cross over Sample size: -9/-9 Primary endpoint: FU duration: |
|
diabetes type 2 | glyburide | not classified | versus No demonstrated result for efficacy | 10 trials | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
Garber, 2006 | glibenclamide vs rosiglitazone (add on MET) | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | | | T1 vs T0 | | | |
Trial | Treatments | Patients | Method |
---|
Garber, 2006 | metformin-glibenclamide 500/2.5 mg tablets (initial daily dose 1000/5 mg) (n=-9) vs. metformin 500 mg plus rosiglitazone 4 mg (initial daily dose 1000-2000 mg + 4 mg, depending on previous treatment) (n=-9) | patients with type 2 diabetes inadequately controlled on metformin monotherapy | double-blind Sample size: -9/-9 Primary endpoint: FU duration: 24 weeks | Garber, 2002 | glyburide 2.5 mg (n=-9) vs. placebo (n=-9) | patients with type 2 diabetes who had failed diet and exercise | double-blind Parallel groups Sample size: -9/-9 Primary endpoint: FU duration: | Vray, 1995 | glibenclamide (2.5 mg X 3/d) (n=-9) vs. placebo (n=-9) | type 2 diabetic outpatients, 40-70 years of age, treated by diet alone or oral anti-diabetic drugs | double-blind Factorial plan Sample size: -9/-9 Primary endpoint: FU duration: | Hermann, 1991 | metformin + glibenclamide (n=-9) vs. metformin (n=-9) metformin, glibenclamide or the combination of both | patients with non-insulin-dependent diabetes mellitus | Parallel groups Sample size: -9/-9 Primary endpoint: FU duration: 6 months | DeFronzo, 1995 | metformin and glyburide (n=-9) vs. metformin (n=-9) metformin and glyburide vs. metformin vs. glyburide | patients with non-insulin-dependent diabetes mellitus | double-blind Sample size: -9/-9 Primary endpoint: FU duration: 29 weeks | Erle, 1999 | low-dose glyburide plus metformin (n=-9) vs. high-dose glyburide alone (n=-9) | | Cross over Sample size: -9/-9 Primary endpoint: FU duration: | Marre (ass), 2002 | metformin-glibenclamide 500 mg/2.5 mg or metformin-glibenclamide 500 mg/5 mg, titrated with the intention to achieve fasting plasma glucose (FPG) < or = 7 mmol/l (n=-9) vs. metformin 500 mg, (n=-9) metformin 500 mg, glibenclamide 5 mg, metformin-glibenclamide 500 mg/2.5 mg or metformin-glibenclamide 500 mg/5 mg | patients with Type 2 diabetes mellitus inadequately controlled by metformin monotherapy | double-blind Parallel groups Sample size: -9/-9 Primary endpoint: FU duration: 16 weeks | Blonde, 2002 | glyburide/metformin 2.5 mg/500 mg (n = 160); or glyburide/metformin 5 mg/500 mg (n = 162) (n=-9) vs. metformin 500 mg (n=-9) glyburide 10 mg b.i.d. (n = 164); metformin 500 mg (n = 153); glyburide/metformin 2.5 mg/500 mg (n = 160); or glyburide/metformin 5 mg/500 mg | patients with inadequate glycaemic control on at least half-maximal dose of sulphonylurea | double-blind Parallel groups Sample size: -9/-9 Primary endpoint: FU duration: 16 weeks | Tosi, 2003 | metformin 400 to 2,400 mg/d + glibenclamide 2.5 to 15 mg/d (n=-9) vs. metformin (500 to 3,000 mg/d), (n=-9) metformin (500 to 3,000 mg/d), glibenclamide (5 to 15 mg/d), or their combination (metformin 400 to 2,400 mg/d + glibenclamide 2.5 to 15 mg/d | | double-blind Cross over Sample size: -9/-9 Primary endpoint: FU duration: 6 months | Garber, 2003 | glyburide/metformin (n=-9) vs. metformin (n=-9) glyburide/metformin tablets vs. metformin or glyburide monotherapy | patients with type 2 diabetes who had inadequate glycemic control [glycosylated hemoglobin A(1C) (A1C), >7% and <12%) with diet and exercise alone | Parallel groups Sample size: -9/-9 Primary endpoint: FU duration: |
|