Page last updated: 2024-10-28

glipizide and Weight Gain

glipizide has been researched along with Weight Gain in 5 studies

Glipizide: An oral hypoglycemic agent which is rapidly absorbed and completely metabolized.
glipizide : An N-sulfonylurea that is glyburide in which the (5-chloro-2-methoxybenzoyl group is replaced by a (5-methylpyrazin-2-yl)carbonyl group. An oral hypoglycemic agent, it is used in the treatment of type 2 diabetes mellitus.

Weight Gain: Increase in BODY WEIGHT over existing weight.

Research Excerpts

ExcerptRelevanceReference
"5% decrease from baseline) with no weight gain and no hypoglycaemic events with alogliptin 12."9.22Comparison of alogliptin and glipizide for composite endpoint of glycated haemoglobin reduction, no hypoglycaemia and no weight gain in type 2 diabetes mellitus. ( Chaudhari, P; Del Prato, S; Fleck, P; Wilson, C, 2016)
"5% decrease from baseline) with no weight gain and no hypoglycaemic events with alogliptin 12."5.22Comparison of alogliptin and glipizide for composite endpoint of glycated haemoglobin reduction, no hypoglycaemia and no weight gain in type 2 diabetes mellitus. ( Chaudhari, P; Del Prato, S; Fleck, P; Wilson, C, 2016)
"Alogliptin monotherapy maintained glycaemic control comparable to that of glipizide in elderly patients with T2DM over 1 year of treatment, with substantially lower risk of hypoglycaemia and without weight gain."5.17Alogliptin versus glipizide monotherapy in elderly type 2 diabetes mellitus patients with mild hyperglycaemia: a prospective, double-blind, randomized, 1-year study. ( Fleck, P; Rosenstock, J; Wilson, C, 2013)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rosenstock, J1
Wilson, C2
Fleck, P2
Del Prato, S1
Chaudhari, P1
Seck, TL1
Engel, SS1
Williams-Herman, DE1
Sisk, CM1
Golm, GT1
Wang, H1
Kaufman, KD1
Goldstein, BJ1
Selam, JL1
Woertz, L1
Lozano, J1
Robinson, M1
Chan, E1
Charles, MA1
Culler, FL1
McKean, LP1
Buchanan, CN1
Caplan, DB1
Meacham, LR1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Multicenter, Double-Blind, Randomized Study to Evaluate the Safety and Efficacy of the Addition of MK0431 Compared With Sulfonylurea Therapy in Patients With Type 2 Diabetes With Inadequate Glycemic Control on Metformin Monotherapy[NCT00094770]Phase 31,172 participants (Actual)Interventional2004-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Change From Baseline in Body Weight at Week 104

Change from baseline at Week 104 is defined as Week 104 minus Week 0. (NCT00094770)
Timeframe: Baseline and Week 104

InterventionKilograms (Least Squares Mean)
Sitagliptin 100 mg-1.6
Glipizide0.7

Change From Baseline in Body Weight at Week 52

Change from baseline at Week 52 is defined as Week 52 minus Week 0. (NCT00094770)
Timeframe: Baseline and Week 52

InterventionKilograms (Least Squares Mean)
Sitagliptin 100 mg-1.5
Glipizide1.1

Change From Baseline in HbA1c at Week 104

HbA1c is measured as percent. Thus, this change from baseline reflects the Week 104 HbA1c percent minus the Week 0 HbA1c percent. (NCT00094770)
Timeframe: Baseline and Week 104

InterventionPercent (Least Squares Mean)
Sitagliptin 100 mg-0.54
Glipizide-0.51

Change From Baseline in HbA1c at Week 52

HbA1c is measured as percent. Thus, this change from baseline reflects the Week 52 HbA1c percent minus the Week 0 HbA1c percent. (NCT00094770)
Timeframe: Baseline and Week 52

InterventionPercent (Least Squares Mean)
Sitagliptin 100 mg-0.67
Glipizide-0.67

Number of Participants With Drug-related LAEs at Week 104

Participants with drug-related (as assessed by an investigator who is a qualified physician according to his/her best clinical judgment) LAEs. (NCT00094770)
Timeframe: Baseline to Week 104

InterventionParticipants (Number)
Sitagliptin 100 mg18
Glipizide21

Hypoglycemic Events at Week 104

Number of participants who reported 1 or more episodes of the adverse experience of hypoglycemia. (NCT00094770)
Timeframe: Baseline to Week 104

,
InterventionParticipants (Number)
Participants with one or more Hypoglycemic AEsTotal number of Hypoglycemic episodesParticipants with no Hypoglycemic AEs
Glipizide199805385
Sitagliptin 100 mg3157557

Hypoglycemic Events at Week 52

Number of participants who reported 1 or more episodes of the adverse experience (AEs) of hypoglycemia. (NCT00094770)
Timeframe: Baseline to Week 52

,
InterventionParticipants (Number)
Participants with one or more Hypoglycemic AEsTotal number of Hypoglycemic episodesParticipants with no Hypoglycemic AEs
Glipizide187657397
Sitagliptin 100 mg2950559

Number of Participants With Clinical Adverse Experiences (CAEs) at Week 104

An adverse experience (AE) is defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the SPONSOR'S product, whether or not considered related to the use of the product. (NCT00094770)
Timeframe: Baseline to Week 104

,
InterventionParticipants (Number)
With CAESWithout CAES
Glipizide480104
Sitagliptin 100 mg452136

Number of Participants With Drug-related CAEs at Week 104

Participants with drug-related (as assessed by an investigator who is a qualified physician according to his/her best clinical judgment) CAEs. (NCT00094770)
Timeframe: Baseline to Week 104

,
InterventionParticipants (Number)
With drug related CAEsWithout drug related CAEs
Glipizide193391
Sitagliptin 100 mg97491

Number of Participants With Laboratory Adverse Experiences (LAEs) at Week 104

A laboratory adverse experience (LAE) is defined as any unfavorable and unintended change in the chemistry of the body temporally associated with the use of the SPONSOR'S product, whether or not considered related to the use of the product. (NCT00094770)
Timeframe: Baseline to Week 104

,
InterventionParticipants (Number)
With LAEsWithout LAEs
Glipizide74510
Sitagliptin 100 mg85503

Number of Participants With Serious CAEs at Week 104

Serious CAEs are any AEs occurring at any dose that; Results in death; or Is life threatening; or Results in a persistent or significant disability/incapacity; or Results in or prolongs an existing inpatient hospitalization; or Is a congenital anomaly/birth defect; or Is a cancer; or Is an overdose. (NCT00094770)
Timeframe: Baseline to Week 104

,
InterventionParticipants (Number)
With serious CAEsWithout serious CAEs
Glipizide73511
Sitagliptin 100 mg64524

Number of Participants With Serious LAEs at Week 104

Serious LAEs are any LAEs occurring at any dose that: results in death; or is life threatening; or results in a persistent or significant disability/incapacity; or results in or prolongs an existing inpatient hospitalization; or is a congenital anomaly/birth defect; or is a cancer; or is an overdose. (NCT00094770)
Timeframe: Baseline to Week 104

,
InterventionParticipants (Number)
With serious LAEsWithout serious LAEs
Glipizide0584
Sitagliptin 100 mg0588

Trials

4 trials available for glipizide and Weight Gain

ArticleYear
Alogliptin versus glipizide monotherapy in elderly type 2 diabetes mellitus patients with mild hyperglycaemia: a prospective, double-blind, randomized, 1-year study.
    Diabetes, obesity & metabolism, 2013, Volume: 15, Issue:10

    Topics: Aged; Aged, 80 and over; Blood Glucose; Diabetes Mellitus, Type 2; Dipeptidyl-Peptidase IV Inhibitor

2013
Comparison of alogliptin and glipizide for composite endpoint of glycated haemoglobin reduction, no hypoglycaemia and no weight gain in type 2 diabetes mellitus.
    Diabetes, obesity & metabolism, 2016, Volume: 18, Issue:6

    Topics: Adult; Aged; Aged, 80 and over; Blood Glucose; Diabetes Mellitus, Type 2; Double-Blind Method; Drug

2016
Sitagliptin more effectively achieves a composite endpoint for A1C reduction, lack of hypoglycemia and no body weight gain compared with glipizide.
    Diabetes research and clinical practice, 2011, Volume: 93, Issue:1

    Topics: Aged; Diabetes Mellitus, Type 2; Dipeptidyl-Peptidase IV Inhibitors; Double-Blind Method; Female; Gl

2011
The use of glipizide combined with intensive insulin treatment for the induction of remissions in new onset adult type I diabetes.
    Autoimmunity, 1993, Volume: 16, Issue:4

    Topics: Adult; Age of Onset; Algorithms; Blood Glucose; C-Peptide; Combined Modality Therapy; Diabetes Melli

1993

Other Studies

1 other study available for glipizide and Weight Gain

ArticleYear
Glipizide treatment of patients with cystic fibrosis and impaired glucose tolerance.
    Journal of pediatric gastroenterology and nutrition, 1994, Volume: 18, Issue:3

    Topics: Adolescent; Adult; Child; Cystic Fibrosis; Female; Glipizide; Glucose Intolerance; Glycated Hemoglob

1994