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The Satiety Effect After Okara Compared to Porridge Eating

T

Tel Aviv Sourasky Medical Center

Status

Unknown

Conditions

Healthy People

Treatments

Dietary Supplement: Nutrigal Okara - 100

Study type

Interventional

Funder types

Other

Identifiers

NCT01075568
TASMC-10-NV-016-CTIL

Details and patient eligibility

About

To examine the satiety effect after eating of Okara.

Full description

This will be a single blind, cross-over design. Study population will include 10 subjects. The patients will be randomly assigned to receive one of two meals, 48 gram Okara or 40 gram (similar caloric value) semolina in two occasions (two visits). After the eating, the subject will stay in a closed room, without watch or any irritation. After three hours, the patient will fill a VAS questionnaire, and will get a standard meal. The meal will be weighed before and after.

Okara is a natural water extracted food grade soy product, contains approximately 35% protein (mfb), and about 43% of dietary fibers.

Enrollment

10 estimated patients

Sex

All

Ages

20 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers
  • Age 20-65 years old
  • Written Informed Consent

Exclusion criteria

  • History of gastro-intestinal surgery
  • On medication that may influence gastric emptying, or medication for weight loss
  • Patient on PPI treatment, H2 Blockers or medication for weight loss
  • Known allergies to soy
  • Pregnancy or breast-feeding
  • Smoking
  • Athletes
  • Metabolic syndrome or diabetes mellitus
  • Family history of metabolic syndrome or diabetes mellitus
  • Weight loss > 2 kg during two months before the study

Trial contacts and locations

1

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Central trial contact

Nachum Vaisman, Prof'

Data sourced from clinicaltrials.gov

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