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Phase 2 N=405 Randomized Treatment

Development of Rational Ways of Medical and Non-medical Treatment Methods for Metabolic Syndrome

Metabolic Syndrome

Enrolled (actual)
405
Serious AEs
15.7%
Results posted
Nov 2015
Primary outcome: Primary: Blood Glucose Level — 6.05; 6.43; 4.58; 14.5 mmole/L

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Xenical, Pionorm, Diroton, Diltiazem, Atorvastatin (Drug); "Analimentary detoxication" (Dietary_supplement)
Age
Adult, Older Adult · 25+ yrs
Sex
All
Sponsor
Nazarbayev University
Primary completion
Dec 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Blood Glucose Level
6.05; 6.43; 4.58; 14.5; 14.6; 5.3
PRIMARY
Systolic/ Diastolic Blood Pressures (mm Hg)
151.2; 152.1; 121.1; 94.1; 96.9; 79.9
SECONDARY
Lipid Profile
5.22; 5.35; 4.9; 0.76; 0.75; 1.22
SECONDARY
Immunoassay Hormones in Blood
22.9; 23.2; 6.5
SECONDARY
Immunoassay Cortisole in Blood
743.8; 751.2; 445.3

Summary

Metabolic syndrome: aetiology, pathogenesis, diagnosis, clinical management and prognosis

Eligibility Criteria

Inclusion Criteria

  • written consent form
  • age> 25 years
  • skinfold thickness > 0, 7 cm BP> 130/85 mm Hg or a patient on antihypertensive medications fasting blood glucose > 6.1 mmole/L, or 2-hour postprandial glucose level > 11.1 mmole/L / or a patient with type 2 diabetes blood cholesterol > 5.6 mmole/L possibility of treatment > 6 months follow-up > 1 year

Exclusion Criteria

  • complete immobilization of a patient (paresis /paralysis)
  • patients with severe concomitant diseases of the kidneys and (or) of the liver
  • early post-operative condition
  • mental illness
  • pregnancy
  • persons who are in prison
  • persons who are in military Armed Forces
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02503865). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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