NCT07627048

Brief Summary

An observational, single-center, prospective study was conducted to examine the impact of CM on the development of T2DM and the personalization of initial SST in patients with newly diagnosed T2DM who had not previously received SST. These patients were hospitalized at the V.P. Demikhov City Clinical Hospital between October 2021 and February 2022 due to hyperglycemia detected incidentally at their place of residence. The sample consisted of men and women aged 18 to 80 years. After hospitalization, the diagnosis of newly diagnosed T2DM was confirmed twice using any available laboratory diagnostic methods: fasting venous blood glucose greater than 7.0 mmol/L or greater than 11.1 mmol/L when randomly determined; glucose greater than 11.1 mmol/L 2 hours after oral administration of 75 g of glucose; and HbA1c greater than 6.5%. After double confirmation of the T2DM diagnosis, 100 patients with newly diagnosed T2DM who had not previously received SST and met the inclusion criteria were included in the study. At the first visit, after assessing patient compliance with the inclusion and exclusion criteria, anamnesis was collected, anthropometric analysis was performed, and intravenous blood was drawn for hormonal (insulin, C-peptide, glucagon, GLP-1) and biochemical blood tests (glucose, HbA1c, TC, LDL, HDL, TG, creatinine, urea, ALT, AST, total bilirubin). Glucagon and GLP-1 levels in the blood were measured on an empty stomach (0 min. point) and 30 minutes after a standard breakfast (30 min. point). Also, at the first visit, in order to assess the composition of the CM, 100 patients underwent stool sampling for 16S rRNA sequencing. At the 2nd visit, as laboratory test results became available, patients were randomized to monotherapy or combination therapy groups depending on the HbA1c level in accordance with the 2019 Algorithms for Specialized Care for Patients with Diabetes Mellitus \[164\]. Metformin was prescribed as monotherapy at a daily dose of 2000 mg (n = 20), and innovative CAPs were added to metformin as combination therapy: DPP-4 inhibitors (n = 20) / GLP-1 arginine (n = 20) / NGLT-2 inhibitors (n = 20) or DPP-4 inhibitors + insulin glargine 300 U/ml (n = 20)/ The effectiveness of the treatment was assessed at the third visit based on HbA1c levels after three months of treatment. If target glycemic levels were not achieved after three months of treatment, the HbA1c levels were adjusted at the third visit based on national recommendations.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2021

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2021

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2021

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 10, 2022

Completed
4.1 years until next milestone

First Submitted

Initial submission to the registry

May 21, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

June 4, 2026

Completed
Last Updated

June 4, 2026

Status Verified

May 1, 2026

Enrollment Period

Same day

First QC Date

May 21, 2026

Last Update Submit

May 29, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Number of participants with domination of different bacterial species in the stool analysis

    3 months

Study Arms (5)

Metformin

Metformin + DPP4-i

Metformin + GLP-1RA

Metformin + SGLT-2i

Metformin + DPP-4i _ Insulin Glargine

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients were hospitalized at the V.P. Demikhov City Clinical Hospital between October 2019 and February 2021 due to hyperglycemia detected incidentally at their place of residence. The sample consisted of men and women aged 18 to 80 years.

You may qualify if:

  • Newly diagnosed T2DM
  • No ketoacidosis
  • Age ≥ 18 years, ≤ 80 years
  • BMI \> 25 kg/m2
  • No history of taking hypoglycemic drugs (HGD)
  • No use of drugs that affect BM composition

You may not qualify if:

  • Presence of type 1 diabetes
  • Presence of chronic gastrointestinal diseases: ulcerative colitis, Crohn's disease, celiac disease, irritable bowel syndrome, multiple intestinal polyposis, chronic pancreatitis with frequent exacerbations (more than 6-7 times per year)
  • Presence of acute gastrointestinal diseases: acute pancreatitis, acute cholecystitis, enteritis, colitis, exacerbation of gastric ulcer or duodenal ulcer
  • Previous gastrointestinal surgery within the last 3 months Gastrointestinal surgery within the last 3 months.
  • Severe infectious diseases (HIV, hepatitis B, hepatitis C, tuberculosis, Covid-19)
  • Glomerular filtration rate (GFR) \< 30 ml/min/1.73 m2
  • Mental illness
  • Alcoholism, drug addiction
  • Pregnancy or lactation
  • Cancer
  • History of blood transfusion, organ transplant, or bone marrow transplant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

State clinical hospital named after V.P. Demikhov

Moscow, Russia

Location

MeSH Terms

Conditions

Diabetes Mellitus, Type 2

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

May 21, 2026

First Posted

June 4, 2026

Study Start

December 1, 2021

Primary Completion

December 1, 2021

Study Completion

April 10, 2022

Last Updated

June 4, 2026

Record last verified: 2026-05

Locations