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Impact of Eccentric Training in Hypoxia With Creatine on Metabolic Control and VO2max in Patients With Type 1 Diabetes - Trial NCT06345612

Access comprehensive clinical trial information for NCT06345612 through Pure Global AI's free database. This phase not specified trial is sponsored by Silesian Centre for Heart Diseases and is currently Recruiting. The study focuses on Type 1 Diabetes. Target enrollment is 28 participants.

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NCT06345612
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behavioral
Trial Details
ClinicalTrials.gov โ€ข NCT06345612
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Impact of Eccentric Training in Hypoxia With Creatine on Metabolic Control and VO2max in Patients With Type 1 Diabetes
Impact of Eccentric Training Conducted in the Conditions of Normobaric Hypoxia, Normoxia and Creatine Supplementation on Metabolic Control, Muscle Strength Level, Maximum Oxygen Consumption (VO2max) in Patients With Type 1diabetes Mellitus

Study Focus

Type 1 Diabetes

hypoxia

Interventional

behavioral

Sponsor & Location

Silesian Centre for Heart Diseases

Zabrze, Poland

Timeline & Enrollment

N/A

Nov 15, 2023

Jul 01, 2025

28 participants

Primary Outcome

Metabolic control of diabetes,Time in range,Time below range,Maximum oxygen consumption (VO2max)

Summary

Exercise plays an important role in treatment of diabetes. In recent years exercise training
 in normobaric hypoxia is used in training programs for athletes and in rehabilitation and
 also commercially. The aim of the study is to assess the impact of eccentric training
 conducted in conditions of normobaric hypoxia or normoxia and creatine supplementation on
 metabolic control: profile and stability of glucose concentration, HbA1c value, hypoglycemia
 and insulin demand, as well as the level of muscle strength, VO2max and anthropometric
 parameters

ICD-10 Classifications

Type 1 diabetes mellitus
Type 1 diabetes mellitus without complications
Type 1 diabetes mellitus with unspecified complications
Type 1 diabetes mellitus with other specified complications
Type 1 diabetes mellitus with multiple complications

Data Source

ClinicalTrials.gov

NCT06345612

Non-Device Trial