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Metformin and Transient Hyperglycemia

Primary Purpose

Acute Lymphoblastic Leukemia, Hyperglycemia, Insulin Resistance

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Metformin
Sponsored by
Children's Hospital Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Lymphoblastic Leukemia focused on measuring Induction chemotherapy, Transient hyperglycemia, Metformin, Acute lymphoblastic leukemia, Insulin resistance, Hyperglycemia, Insulin

Eligibility Criteria

10 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ALL patients on induction chemotherapy who develop transient hyperglycemia(definition of transient hyperglycemia: random blood glucose > 200 mg/dL x 2)
  • Adequate renal function (serum Cr < 1.5 mg/dL in males, < 1.2 mg/dL in females)
  • Adequate hepatic function (AST < 5x upper limit of normal)

Exclusion Criteria:

  • Patients with known diagnosis of diabetes or those that are already on oral hypoglycemic agents or insulin
  • Allergy to metformin or any component of the formulation
  • Patients with pancreatitis (lipase level > 300 Units/L)
  • Patients with active infection (positive blood culture within 48 hours of study registration)
  • Patients with hemodynamic instability (PICU status, need for vasopressors within 48 hours of study entry)
  • Elevated hemoglobin A1c (greater than 6.0%)

Sites / Locations

  • Children's Hospital Los Angeles

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Metformin and insulin therapy

Arm Description

Up to 30-40 patients will be in the prospectively recruited treatment group, which will receive both metformin and insulin therapy for transient hyperglycemia

Outcomes

Primary Outcome Measures

Length of Insulin Therapy (Days)

Secondary Outcome Measures

Serum Fructosamine Level
Hemoglobin A1c

Full Information

First Posted
November 30, 2011
Last Updated
January 20, 2015
Sponsor
Children's Hospital Los Angeles
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1. Study Identification

Unique Protocol Identification Number
NCT01486043
Brief Title
Metformin and Transient Hyperglycemia
Official Title
Metformin as an Adjunctive Therapy For Transient Hyperglycemia in Patients With Acute Lymphoblastic Leukemia During Induction Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Terminated
Why Stopped
The research project was terminated due to lower than projected patient recruitment within the period of time allowed for the study.
Study Start Date
December 2011 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital Los Angeles

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether metformin is an effective adjunctive treatment for transient hyperglycemia in patients with acute lymphoblastic leukemia (ALL) undergoing induction chemotherapy
Detailed Description
ALL is the most common childhood cancer, representing one fourth of all cancers diagnosed under the age of 15 years. One of the most common side effects of ALL chemotherapy is transient hyperglycemia. Patients that develop this complication require treatment with insulin via injections to prevent severe medical complications such as dehydration, weight loss, ketoacidosis and life-threatening infections. Although insulin therapy is effective, it adds a lot of physical and psychological burden to patients because multiple daily insulin injections are required to achieve adequate blood glucose control. In this pilot study, investigators aim to examine the effectiveness of metformin as an adjunctive treatment for transient hyperglycemia. Investigators will be comparing two groups of subjects (up to 40 subjects per group). Patients in the treatment group will be prospectively recruited, and they will be treated with metformin in addition to insulin therapy. Investigators will compare the treatment group to a historical control group acquired via chart review. These patients will have been treated with insulin alone. Statistical comparison will be made between the two groups in terms of the length of insulin treatment, the total daily dose of insulin required, number of insulin injections, hemoglobin A1c level (measure of glycemic control over preceding 8- 12 weeks), and fructosamine level (measure of glycemic control over preceding 2-3 weeks). Investigators hypothesize that the use of metformin will result in fewer numbers of insulin injections and fewer days of insulin therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Lymphoblastic Leukemia, Hyperglycemia, Insulin Resistance, Diabetes Mellitus
Keywords
Induction chemotherapy, Transient hyperglycemia, Metformin, Acute lymphoblastic leukemia, Insulin resistance, Hyperglycemia, Insulin

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metformin and insulin therapy
Arm Type
Experimental
Arm Description
Up to 30-40 patients will be in the prospectively recruited treatment group, which will receive both metformin and insulin therapy for transient hyperglycemia
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Glucophage, Metformin HCl
Intervention Description
All subjects will be started on metformin 500 mg orally twice daily. The dose will be increased by 500 mg weekly as tolerated until subjects' blood glucoses are well controlled or until the patient reaches metformin 1000 mg PO BID.
Primary Outcome Measure Information:
Title
Length of Insulin Therapy (Days)
Time Frame
During the 30 days of induction chemotherapy (plus or minus 2 weeks)
Secondary Outcome Measure Information:
Title
Serum Fructosamine Level
Time Frame
At 1 month
Title
Hemoglobin A1c
Time Frame
At 1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ALL patients on induction chemotherapy who develop transient hyperglycemia(definition of transient hyperglycemia: random blood glucose > 200 mg/dL x 2) Adequate renal function (serum Cr < 1.5 mg/dL in males, < 1.2 mg/dL in females) Adequate hepatic function (AST < 5x upper limit of normal) Exclusion Criteria: Patients with known diagnosis of diabetes or those that are already on oral hypoglycemic agents or insulin Allergy to metformin or any component of the formulation Patients with pancreatitis (lipase level > 300 Units/L) Patients with active infection (positive blood culture within 48 hours of study registration) Patients with hemodynamic instability (PICU status, need for vasopressors within 48 hours of study entry) Elevated hemoglobin A1c (greater than 6.0%)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jamie R Wood, M.D.
Organizational Affiliation
Children's Hospital Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
6454771
Citation
Pui CH, Burghen GA, Bowman WP, Aur RJ. Risk factors for hyperglycemia in children with leukemia receiving L-asparaginase and prednisone. J Pediatr. 1981 Jul;99(1):46-50. doi: 10.1016/s0022-3476(81)80955-9.
Results Reference
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PubMed Identifier
15700246
Citation
Baillargeon J, Langevin AM, Mullins J, Ferry RJ Jr, DeAngulo G, Thomas PJ, Estrada J, Pitney A, Pollock BH. Transient hyperglycemia in Hispanic children with acute lymphoblastic leukemia. Pediatr Blood Cancer. 2005 Dec;45(7):960-3. doi: 10.1002/pbc.20320.
Results Reference
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PubMed Identifier
19260096
Citation
Lowas SR, Marks D, Malempati S. Prevalence of transient hyperglycemia during induction chemotherapy for pediatric acute lymphoblastic leukemia. Pediatr Blood Cancer. 2009 Jul;52(7):814-8. doi: 10.1002/pbc.21980.
Results Reference
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PubMed Identifier
12350366
Citation
Howard SC, Pui CH. Endocrine complications in pediatric patients with acute lymphoblastic leukemia. Blood Rev. 2002 Dec;16(4):225-43. doi: 10.1016/s0268-960x(02)00042-5.
Results Reference
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PubMed Identifier
19394046
Citation
Sonabend RY, McKay SV, Okcu MF, Yan J, Haymond MW, Margolin JF. Hyperglycemia during induction therapy is associated with poorer survival in children with acute lymphocytic leukemia. J Pediatr. 2009 Jul;155(1):73-8. doi: 10.1016/j.jpeds.2009.01.072. Epub 2009 Apr 25.
Results Reference
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Metformin and Transient Hyperglycemia

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