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

NCT ID: NCT02503865

Last Updated: 2015-11-30

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1/PHASE2

Total Enrollment

351 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-01-31

Study Completion Date

2014-12-31

Brief Summary

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

Detailed Description

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Purpose: To create the complex scientifically proved concept of Metabolic syndrome (МS) development based on elaboration of the new methods of clinical diagnostics of МS components and highly effective МS clinical management in comparative studying of clinical, laboratory and cost effectiveness.

Participants and methods: This clinical study included 351 adults (184 female) in the Scientific research institute of cardiology and internal diseases (Almaty, the Republic of Kazakhstan). Statistical analysis was performed using Microsoft Excel-2008 in updating Lapach, Chubenko et al (2000) and SPSS for Windows v.17.0.

Conditions

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Metabolic Syndrome

Keywords

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Metabolic syndrome Diabetes mellitus, Hypertension Overweight analimentary detoxication

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Conventional Patient group

Xenical, Pionorm, Diroton, Diltiazem, Atorvastatin

Group Type ACTIVE_COMPARATOR

Xenical, Pionorm, Diroton, Diltiazem, Atorvastatin

Intervention Type DRUG

Xenical (Orlistat) - 120 mg/day in integration of Pionorm (Pioglitazone hydrochlorid) - 30 mg/day, Diroton (Lizinopril) - 20 mg/day, Diltiazem - 90 mg/day, Atorvastatin (Liprimar) - 40 mg/day

"Analimentary detoxication" Weight loss

Vegetables and salt diet

Group Type EXPERIMENTAL

"Analimentary detoxication"

Intervention Type DIETARY_SUPPLEMENT

Vegetable and salt diet

Healthy people

64 healthy people

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Xenical, Pionorm, Diroton, Diltiazem, Atorvastatin

Xenical (Orlistat) - 120 mg/day in integration of Pionorm (Pioglitazone hydrochlorid) - 30 mg/day, Diroton (Lizinopril) - 20 mg/day, Diltiazem - 90 mg/day, Atorvastatin (Liprimar) - 40 mg/day

Intervention Type DRUG

"Analimentary detoxication"

Vegetable and salt diet

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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Conventional Patient group Experimental Patient group

Eligibility Criteria

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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
Minimum Eligible Age

25 Years

Maximum Eligible Age

74 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Institute Of Cardiology & Internal Diseases, Kazakhstan

OTHER_GOV

Sponsor Role collaborator

Nazarbayev University

OTHER

Sponsor Role lead

Responsible Party

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Kuat Oshakbayev

Primary investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tabynbayev Nariman, Professor

Role: STUDY_DIRECTOR

Nazarbayev University

Locations

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Republican Scientific Center for Emergency Medicine

Astana, Astana, Kazakhstan

Site Status

Countries

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Kazakhstan

References

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Penn L, White M, Lindstrom J, den Boer AT, Blaak E, Eriksson JG, Feskens E, Ilanne-Parikka P, Keinanen-Kiukaanniemi SM, Walker M, Mathers JC, Uusitupa M, Tuomilehto J. Importance of weight loss maintenance and risk prediction in the prevention of type 2 diabetes: analysis of European Diabetes Prevention Study RCT. PLoS One. 2013;8(2):e57143. doi: 10.1371/journal.pone.0057143. Epub 2013 Feb 25.

Reference Type BACKGROUND
PMID: 23451166 (View on PubMed)

Berk KA, Buijks H, Ozcan B, Van't Spijker A, Busschbach JJ, Sijbrands EJ. The Prevention Of WEight Regain in diabetes type 2 (POWER) study: the effectiveness of adding a combined psychological intervention to a very low calorie diet, design and pilot data of a randomized controlled trial. BMC Public Health. 2012 Nov 23;12:1026. doi: 10.1186/1471-2458-12-1026.

Reference Type BACKGROUND
PMID: 23176668 (View on PubMed)

Browning JD, Baxter J, Satapati S, Burgess SC. The effect of short-term fasting on liver and skeletal muscle lipid, glucose, and energy metabolism in healthy women and men. J Lipid Res. 2012 Mar;53(3):577-586. doi: 10.1194/jlr.P020867. Epub 2011 Dec 3.

Reference Type RESULT
PMID: 22140269 (View on PubMed)

Oshakbayev K, Dukenbayeva B, Togizbayeva G, Durmanova A, Gazaliyeva M, Sabir A, Issa A, Idrisov A. Weight loss technology for people with treated type 2 diabetes: a randomized controlled trial. Nutr Metab (Lond). 2017 Jan 31;14:11. doi: 10.1186/s12986-017-0163-9. eCollection 2017.

Reference Type DERIVED
PMID: 28163748 (View on PubMed)

Other Identifiers

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0103RK00112

Identifier Type: -

Identifier Source: org_study_id