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Trial to Evaluate the Effect of Plantago Ovata Husk in the Remission of Metabolic Syndrome in Children and Adolescents

R

Rottapharm

Status and phase

Terminated
Phase 2

Conditions

Metabolic Syndrome

Treatments

Drug: Placebo
Drug: Ispaghula husk

Study type

Interventional

Funder types

Industry

Identifiers

NCT00748787
PLAN-EC-PEDIA-01
EudraCT number. 2007-005019-25

Details and patient eligibility

About

The metabolic syndrome represents a constellation of risk factors associated to the abdominal obesity that includes insulin resistance, lipids alterations, high blood pressure etc. Several studies support the hypothesis that the intake of soluble fiber might have a positive effect in the improvement of such of these risk factors.

So that, the aim of this study is to evaluate the efficacy of Ispaghula husk in the remission of metabolic syndrome in children between 10 to 16 years old.

Full description

The prevalence of the metabolic syndrome is increasing in the last decade as well in adult people as in children and adolescents. The early diagnosis and treatment measures could be very important in order to reduce the cardiovascular risk in such populations.

Ispaghula husk could be efficacious to reach the remission of the syndrome due to its effects in several important lipidic parameters.

The study will consist in the treatment with Ispaghula husk during 4 months in patients with metabolic syndrome. The main variable is the remission of the metabolic syndrome following the IDF(International Diabetes Federation) criteria specifics for children.

Enrollment

19 patients

Sex

All

Ages

10 to 16 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children between 10 to 16 years old with diagnostic criteria of metabolic syndrome following the IDF criteria:

    1. Waist circumference > or equal to percentile 90 according the age.
    2. Presence of 2 or more of following factors: systolic blood pressure > or equal 130 mmHg or diastolic > or equal to 85 mmHg, or treated hypertension
    3. Cholesterol HDL < 1.03 mmol/l or treatment with drugs to increase cHDL
    4. Glucose blood levels > 5.6 mmol/l or type II diabetes diagnosed treated or no.

Exclusion criteria

  • Loss of body weight > 3kg in the last 2 months
  • Waist circumference 10 cm higher of 90 percentile according to the age
  • Intake of fiber, aven supplements or phytosterols in the last 2 months
  • Glycosylate haemoglobin >7% in the time of inclusion
  • Systolic blood pressure > 145 mmHg or Diastolic blood pressure >95 mmHg.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

19 participants in 2 patient groups, including a placebo group

1
Experimental group
Treatment:
Drug: Ispaghula husk
2
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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