Diabetes Mellitus, Type 2NCT00225225
Rosiglitazone-Induced Weight Gain
A study testing Rosiglitazone and dietary recommendation for weight maintenance in people with Diabetes Mellitus, Type 2, run by Stanford University at 1 site in United States.
Trial summary
Given the high prevalence of type 2 diabetes and the 2- to 4-fold increased risk of fatal and non-fatal coronary heart disease events in these patients, long-term glycemic control is of great importance. Read more about this study
- Who is it for?
- Ages 20 to 75 years
- Conditions the study is for
- Diabetes Mellitus, Type 2
- What is being tested?
- Rosiglitazone and dietary recommendation for weight maintenance
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 45 participants
- Where
- 1 siteUnited States
- Study dates
- Oct 2002to Sep 2005
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Inclusion Criteria:- 1) age between 30 and 70 years old, 2) normal chemical screening battery, 2) BMI less than 36 kg/M2, 3) non-controlled type 2 DM, defined by a fasting plasma glucose between 160 and 220 mg/dl, 4) individuals should be on a stable dose of sulfonylurea for at least one month prior to the enrollment. Exclusion Criteria:- 1) liver enzymes 2.5 times above normal values, 2) chronic inflammatory, neoplastic disease, 3) subjects with clinical evidence of congestive heart failure.
Trial locations and contacts
1 site in 1 country.
United States1 site
Stanford University School of Medicine
Stanford, California, 94305
About this study
Given the high prevalence of type 2 diabetes and the 2- to 4-fold increased risk of fatal and non-fatal coronary heart disease events in these patients, long-term glycemic control is of great importance. TZDs improves glycemic control in patients with type 2 DM as well as enhances their insulin-mediated glucose disposal. However, the improvement of glycemic control seen with TZDs may be blunted in the long run by weight gain.
Previous data on weight gain during TZD therapy in patients with type 2 DM is very sparse. It is generally assumed that an increase in adipocyte differentiation is the cause of weight gain in association with TZD treatment which may limit their use. Increased body weight assumed to compromise the positive effects of treatment. There is also a theoretical concern that, with the development of new adipocytes, future weight loss may be difficult.
Read more
However, if weight gain is primarily due to failure to adjust caloric intake in proportion to the decrease in urinary glucose loss, it is totally preventable. It has been previously shown that improvement of glycemia favored weight gain by decreasing the energy loss in the urine as glucose. Severity of weight gain appears to be proportional to the level of glycemic control achieved.
The overall goal of the proposed research is to provide the experimental evidence for the later alternative by showing that the modest weight gain that takes place in association with effective rosiglitazone treatment of hyperglycemic patients with type 2 DM is primarily due to its therapeutic efficacy. More specifically, by decreasing the caloric intake in proportion to a decrease in urinary glucose loss associated with improved glycemic control, we will be able to prevent significant weight gain following Rosiglitazone treatment. In order to provide an optimal dietary modification that can be universally applied to TZD-treated patients in clinical practice, we will have a group with a fixed amount of caloric restriction per day. It will be the first randomized controlled trial of a potential strategy for prevention of weight gain associated with thiazolidinediones.
Read the detailed description
Study Design Randomized, controlled trial. Volunteers for the study will be recruited by advertisements in the local newspapers as well as through Stanford University e-mail. All studies will occur at Stanford General Clinical Research Center (GCRC).
At baseline, enrolled candidates will be required to keep a daily food and beverage record for 2 weeks as well as blood sugar log of at least 2 measurements a day (fasting and pre-dinner). Candidates will have an initial nutrition/diabetes consult with dietitian. They also will be asked to do a 24-hour urine collection once a week (2 times during the 2 week period) for quantitative assessment of glucosuria. During those 2 weeks individuals will come for GCRC outpatient visit once a week for weight, blood pressure, and blood sugar check.
After the initial two weeks, all individuals will undergo a meal profile test, after a 12-hour overnight fast, which consists of measurement of daylong plasma glucose, free fatty acids, and insulin responses to standard meals. Food for the test will be prepared by GCRC Metabolic kitchen. In order to assess the degree of postprandial and day-long hyperinsulinemia and the benefits of rosiglitazone on the metabolic abnormalities in patients with poor glycemic control, we plan to measure plasma glucose, free fatty acids, and insulin concentrations before 8 am and at hourly intervals for four hours after breakfast at 8 am and four hours after lunch at noon in response to identical test meals containing (as percentage of calories) 15% protein, 40% fat, and 45% carbohydrate. Baseline blood samples for fasting lipid and lipoprotein concentrations will be obtained after an overnight fast on the day of the meal profile. Cholesterol and lipoprotein subclasses will be analyzed by VAP-II method which is based on continuous enzymatic analysis of cholesterol and lipoprotein classes separated by a single vertical spin centrifugation using a controlled-dispersion flow analyzer. Hemoglobin A1C will be measured by an affinity chromography assay at baseline and at the end of the study.
Randomization protocol. After completion of the Meal Profile test all subjects will be started on Rosiglitazone for improvement of their glycemic control and randomized to one of the three groups (15 subjects in each group):
- Continuation of the current diet.
- Reduced calorie diet. Amount of reduced calories will be calculated proportionally to the calories lost via glucosuria.
- Fixed calorie reduction diet. Reduction of daily caloric intake by 500 kcal. Rosiglitazone will be given at 4 mg for the first 4 weeks, and if tolerated, increased to 8 mg for the duration of the study. All candidates will have counseling on general meal plan with the nutritionist.
Follow-up. Subjects will be followed for 4 months. They will come to the GCRC twice a month for weight, blood pressure, blood sugar checks, and for nutrition follow-up.
End of the study measurements and clinical procedures: meal profile, lipid panel, 24-hour urine collection will be done at the end of 4 month follow-up period. Liver function tests will be done at the baseline, 4, 8, 12, and 16 weeks while on Rosiglitazone.
Outcomes: we expect to demonstrate at the end of the study that modification of the diet prevents weight gain in Rosiglitazone treated patients and to offer the optimal dietary interventions that could be applied in TZD-treated patients to minimize weight gain while effectively treating DM and insulin resistance.
Inclusion / Exclusion Inclusion criteria: 1) age between 30 and 70 years old, 2) normal chemical screening battery, 2) BMI less than 36 kg/M2, 3) non-controlled type 2 DM, defined by a fasting plasma glucose between 160 and 220 mg/dl, 4) individuals should be on a stable dose of sulfonylurea for at least one month prior to the enrollment.
Exclusion criteria: 1) liver enzymes 2.5 times above normal values, 2) chronic inflammatory, neoplastic disease, 3) subjects with clinical evidence of congestive heart failure.
- Conditions
- Diabetes Mellitus, Type 2
- Being tested
- Rosiglitazone, dietary recommendation for weight maintenance
- Medical subject headings
- Diabetes Mellitus, Type 2
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
RosiglitazoneDrug
dietary recommendation for weight maintenanceBehavioural
| Study group | Role | What they receive |
|---|---|---|
| fixed calorie (500 kcal) Reduction | Active comparator | Not described Receives: Drug: Rosiglitazone |
| Control (no diet change) | Placebo comparator | Not described Receives: Drug: Rosiglitazone; Behavioral: dietary recommendation for weight maintenance |
What is being measured
The primary outcome is the main question the study is designed to answer.
modification of the diet prevents weight gain.
Secondary outcomes (1)
develop specific dietary recommendations
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Sep 2005 (estimated)
- Study startOct 2002
- Primary completionSep 2005
- Study completionSep 2005
Why it stopped: due to published data on Rosiglitazone
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Diabetes Mellitus, Type 2Studies of the same condition, open and under way.
- More trials run by Stanford UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 45 participants (actual)
Sponsor and investigators
- Lead sponsor
- Stanford University
- Sponsor type
- University, hospital or other
- Collaborators
- GlaxoSmithKline
- Responsible party
- Principal investigator, Marina Basina, Stanford University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00225225
- Sponsor's protocol ID
- 96242
- Other IDs
- SPO# 34216
- Status last verified
- Oct 2016
- First submitted
- 21 Sep 2005
- Last updated
- 20 Oct 2016
- Results posted
- No
Publications
Vasudevan AR, Balasubramanyam A. Thiazolidinediones: a review of their mechanisms of insulin sensitization, therapeutic potential, clinical efficacy, and tolerability. Diabetes Technol Ther. 2004 Dec;6(6):850-63. doi: 10.1089/dia.2004.6.850.
PubMed 15684639Asnani S, Richard BC, Desouza C, Fonseca V. Is weight loss possible in patients treated with thiazolidinediones? Experience with a low-calorie diet. Curr Med Res Opin. 2003;19(7):609-13. doi: 10.1185/030079903125002306.
PubMed 14606983Camp HS. Thiazolidinediones in diabetes: current status and future outlook. Curr Opin Investig Drugs. 2003 Apr;4(4):406-11.
PubMed 12808879Viberti GC. Rosiglitazone: potential beneficial impact on cardiovascular disease. Int J Clin Pract. 2003 Mar;57(2):128-34.
PubMed 12661797
Study at a glance
From the registry record, last updated by the sponsor on 20 Oct 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Rosiglitazone-Induced Weight Gain
- ClinicalTrials.gov ID
- NCT00225225
- Acronym / sponsor ID
- 96242
- Conditions
- Diabetes Mellitus, Type 2
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: due to published data on Rosiglitazone
- Enrolment
- 45 participants (actual)
- Lead sponsor
- Stanford UniversityUniversity, hospital or other
- Collaborators
- GlaxoSmithKline
- Study start
- Oct 2002
- Primary completion
- Sep 2005 (actual)
- Study completion
- Sep 2005 (actual)
- First posted
- 23 Sep 2005 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Given the high prevalence of type 2 diabetes and the 2- to 4-fold increased risk of fatal and non-fatal coronary heart disease events in these patients, long-term glycemic control is of great importance. TZDs improves glycemic control in patients with type 2 DM as well as enhances their insulin-mediated glucose disposal. However, the improvement of glycemic control seen with TZDs may be blunted in the long run by weight gain.
Previous data on weight gain during TZD therapy in patients with type 2 DM is very sparse. It is generally assumed that an increase in adipocyte differentiation is the cause of weight gain in association with TZD treatment which may limit their use. Increased body weight assumed to compromise the positive effects of treatment. There is also a theoretical concern that, with the development of new adipocytes, future weight loss may be difficult.
However, if weight gain is primarily due to failure to adjust caloric intake in proportion to the decrease in urinary glucose loss, it is totally preventable. It has been previously shown that improvement of glycemia favored weight gain by decreasing the energy loss in the urine as glucose. Severity of weight gain appears to be proportional to the level of glycemic control achieved.
The overall goal of the proposed research is to provide the experimental evidence for the later alternative by showing that the modest weight gain that takes place in association with effective rosiglitazone treatment of hyperglycemic patients with type 2 DM is primarily due to its therapeutic efficacy. More specifically, by decreasing the caloric intake in proportion to a decrease in urinary glucose loss associated with improved glycemic control, we will be able to prevent significant weight gain following Rosiglitazone treatment. In order to provide an optimal dietary modification that can be universally applied to TZD-treated patients in clinical practice, we will have a group with a fixed amount of caloric restriction per day. It will be the first randomized controlled trial of a potential strategy for prevention of weight gain associated with thiazolidinediones.
Detailed description
Study Design Randomized, controlled trial. Volunteers for the study will be recruited by advertisements in the local newspapers as well as through Stanford University e-mail. All studies will occur at Stanford General Clinical Research Center (GCRC).
At baseline, enrolled candidates will be required to keep a daily food and beverage record for 2 weeks as well as blood sugar log of at least 2 measurements a day (fasting and pre-dinner). Candidates will have an initial nutrition/diabetes consult with dietitian. They also will be asked to do a 24-hour urine collection once a week (2 times during the 2 week period) for quantitative assessment of glucosuria. During those 2 weeks individuals will come for GCRC outpatient visit once a week for weight, blood pressure, and blood sugar check.
After the initial two weeks, all individuals will undergo a meal profile test, after a 12-hour overnight fast, which consists of measurement of daylong plasma glucose, free fatty acids, and insulin responses to standard meals. Food for the test will be prepared by GCRC Metabolic kitchen. In order to assess the degree of postprandial and day-long hyperinsulinemia and the benefits of rosiglitazone on the metabolic abnormalities in patients with poor glycemic control, we plan to measure plasma glucose, free fatty acids, and insulin concentrations before 8 am and at hourly intervals for four hours after breakfast at 8 am and four hours after lunch at noon in response to identical test meals containing (as percentage of calories) 15% protein, 40% fat, and 45% carbohydrate. Baseline blood samples for fasting lipid and lipoprotein concentrations will be obtained after an overnight fast on the day of the meal profile. Cholesterol and lipoprotein subclasses will be analyzed by VAP-II method which is based on continuous enzymatic analysis of cholesterol and lipoprotein classes separated by a single vertical spin centrifugation using a controlled-dispersion flow analyzer. Hemoglobin A1C will be measured by an affinity chromography assay at baseline and at the end of the study.
Randomization protocol. After completion of the Meal Profile test all subjects will be started on Rosiglitazone for improvement of their glycemic control and randomized to one of the three groups (15 subjects in each group):
- Continuation of the current diet.
- Reduced calorie diet. Amount of reduced calories will be calculated proportionally to the calories lost via glucosuria.
- Fixed calorie reduction diet. Reduction of daily caloric intake by 500 kcal. Rosiglitazone will be given at 4 mg for the first 4 weeks, and if tolerated, increased to 8 mg for the duration of the study. All candidates will have counseling on general meal plan with the nutritionist.
Follow-up. Subjects will be followed for 4 months. They will come to the GCRC twice a month for weight, blood pressure, blood sugar checks, and for nutrition follow-up.
End of the study measurements and clinical procedures: meal profile, lipid panel, 24-hour urine collection will be done at the end of 4 month follow-up period. Liver function tests will be done at the baseline, 4, 8, 12, and 16 weeks while on Rosiglitazone.
Outcomes: we expect to demonstrate at the end of the study that modification of the diet prevents weight gain in Rosiglitazone treated patients and to offer the optimal dietary interventions that could be applied in TZD-treated patients to minimize weight gain while effectively treating DM and insulin resistance.
Inclusion / Exclusion Inclusion criteria: 1) age between 30 and 70 years old, 2) normal chemical screening battery, 2) BMI less than 36 kg/M2, 3) non-controlled type 2 DM, defined by a fasting plasma glucose between 160 and 220 mg/dl, 4) individuals should be on a stable dose of sulfonylurea for at least one month prior to the enrollment.
Exclusion criteria: 1) liver enzymes 2.5 times above normal values, 2) chronic inflammatory, neoplastic disease, 3) subjects with clinical evidence of congestive heart failure.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| fixed calorie (500 kcal) Reduction | Active comparator | Drug: Rosiglitazone |
| Control (no diet change) | Placebo comparator | Drug: Rosiglitazone, Behavioral: dietary recommendation for weight maintenance |
Who may qualify
- Ages
- 20 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Rosiglitazone | Drug | Control (no diet change), fixed calorie (500 kcal) Reduction |
| dietary recommendation for weight maintenance | Behavioural | Control (no diet change) |
Primary outcome
modification of the diet prevents weight gain.
1 secondary outcome
develop specific dietary recommendations
Results and safety
The study was stopped early (reason given: due to published data on Rosiglitazone). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Oct 2016.
- Background: PubMed 15684639Vasudevan AR, Balasubramanyam A. Thiazolidinediones: a review of their mechanisms of insulin sensitization, therapeutic potential, clinical efficacy, and tolerability. Diabetes Technol Ther. 2004 Dec;6(6):850-63. doi: 10.1089/dia.2004.6.850.
- Background: PubMed 14606983Asnani S, Richard BC, Desouza C, Fonseca V. Is weight loss possible in patients treated with thiazolidinediones? Experience with a low-calorie diet. Curr Med Res Opin. 2003;19(7):609-13. doi: 10.1185/030079903125002306.
- Background: PubMed 12808879Camp HS. Thiazolidinediones in diabetes: current status and future outlook. Curr Opin Investig Drugs. 2003 Apr;4(4):406-11.
- Background: PubMed 12661797Viberti GC. Rosiglitazone: potential beneficial impact on cardiovascular disease. Int J Clin Pract. 2003 Mar;57(2):128-34.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Rosiglitazone and dietary recommendation for weight maintenance in people with Diabetes Mellitus, Type 2, run by Stanford University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 20 Oct 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: due to published data on Rosiglitazone). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
modification of the diet prevents weight gain.. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00225225, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Oct 2016.