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Not yet recruiting NCT05925933

High Protein Diet on Transcriptomic, Metabolomics, Hepatic and Pancreatic Fat Anatomy and Physiology in Asian Indians With Pre-diabetes

No phase Interventional Pre-diabetes

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Intervention.
Who it may be relevant to
Registry conditions: Pre-diabetes. Basic parameters: 18 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of High Protein Diet on Transcriptomic Regulations, Plasma Metabolomics, Hepatic and Pancreatic Fat Anatomy and Physiology in Asian Indians With Pre-diabetes

Overview

Diabetes/ prediabetes is a substantial problem in India not only because it itself can be associated with morbidities such as coronary artery disease but also because it is a point of importance for the prevention of other diseases. It is not clear if a high protein calorie diet in the Indian population associated with a heightened tendency for prediabetes, metabolic syndrome, atherosclerosis and dysmetabolic state etc. could, besides lifestyle factors, be related to diet, or interaction between the two. The analysis of whole blood transcriptomes and plasma metabolomics profiles may be a potentially useful tool for the assessment of metabolic health status. The proposed study is the first to perform a detailed gene expression profiling with the use of next-generation sequencing technology to assess the differences in molecular mechanisms in the peripheral blood of subjects with prediabetes.

Detailed description

This study will be conducted at the outpatient department of the National Diabetes, Obesity and Cholesterol Foundation (N-DOC), Diabetes Foundation (India) (DFI)and Fortis-C-DOC, Centre of Excellence for Diabetes, Metabolic Diseases and Endocrinology, New Delhi, India.

Experimental Protocol: In this study, a total of 60 subjects with pre-diabetes and 60 age and body mass index, and gender-matched controls (age 18-40 years) will be recruited. They will be randomized to an equicaloric normal diet (carbohydrates 60%, protein 15%, and fat 25%) or a high protein diet (carbohydrates 45%, protein 29%, and fat 26%) over 8-week periods. All assessments as done on day 1 will be repeated at day 60.

Interventions

  • Other Intervention
    high protein diet (carbohydrates 45%, protein 29%, and fat 26%) over 8-week periods.

Primary outcome measures

  • Body Mass Index [Time frame: 6 Months]
  • Body Fat [Time frame: 2 MONTHS]
  • Liver Fat [Time frame: 2 Months]
  • Next Generation sequencing [Time frame: 06 MONTHS]
  • Pancreatic fat [Time frame: 06 MONTHS]
  • RNA Extraction [Time frame: 06 MONTHS]
  • Metabolomics profile [Time frame: 06 MONTHS]

Eligibility criteria

Exclusion criteria

  • Acute infections and advanced end-organ damage.
  • History of hepatitis or pancreatitis, abnormal liver and renal function tests.
  • Recent (<3 months) changes in weight (≥5%) and/or weight changing medications.
  • Subjects with metallic implants, pacemaker leads, radioactive seeds or surgical staples in the body.

Inclusion criteria

Cases:

  • Age 18 to 50 years. Subjects with pre-diabetes on oral glucose tolerance test (OGTT)
  • Fasting blood glucose≥100mg/dl and <126 mg/dl or 2-h plasma glucose ≥140mg/dl and <200mg/dl (after ingestion of 75 grams of anhydrous oral glucose) or both.

Controls:

  • Age 18 to 50 years. Normoglycemia by OGTT
  • Fasting blood glucose <100mg/dl and 2-h plasma glucose <140mg/dl (after ingestion of 75 gram of anhydrous oral glucose).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT05925933 · DFI/DST/2023

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗