Effects of a Ketogenic Diet on PCOS Outcomes

Sponsor
University of Padova (Other)
Overall Status
Completed
CT.gov ID
NCT04163120
Collaborator
University of Palermo (Other), Universita di Verona (Other), Vita-Salute San Raffaele University (Other)
14
1
1
3.9
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Study Details

Study Description

Brief Summary

The aim of the study is to investigate the effects of a low calorie Mediterranean ketogenic diet on Polycystic Ovary Syndrome (PCOS) related outcomes.

Condition or Disease Intervention/Treatment Phase
  • Other: Low calorie Mediterranean ketogenic diet with phytoextracts (KEMEPHY)
N/A

Detailed Description

Fourteen overweight women with diagnosis of Polycystic Ovary Syndrome (PCOS) will undergo to a low calorie ketogenic Mediterranean diet with phyoextracts (KEMEPHY) for 12 week. Changes in body weight, body mass index (BMI), fat body mass (FBM), lean body mass (LBM), visceral adipose tissue (VAT), insulin, glucose, HOMA-IR, total cholesterol, low density lipoprotein (LDL), high density lipoprotein (HDL(, triglycerides (TGs), total and free testosterone, luteinizing hormone (LH), follicle stimulating hormone (FSH); dehydroepiandrosterone sulfate (DHEAs), estradiol, progesterone, sex hormone binding globulin (SHBG) and Ferriman Gallwey score will be evaluated.

Study Design

Study Type:
Interventional
Actual Enrollment :
14 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Single arm studySingle arm study
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of a Low Calorie Mediterranean Ketogenic Diet in Women With Polycystic Ovary Syndrome
Actual Study Start Date :
Jan 1, 2017
Actual Primary Completion Date :
Mar 1, 2017
Actual Study Completion Date :
May 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

In this single arm study subjects follow a low calorie mediterranean ketogenci diet

Other: Low calorie Mediterranean ketogenic diet with phytoextracts (KEMEPHY)
The KEMEPHY diet (24-29) is a Mediterranean low calories ketogenic protocol (about 1000/1100 Kcal/day) with the use of some phytoextracts. During this protocol subjects are allowed to eat with no limits green leafy vegetables, cruciferous, zucchini, cucumbers and eggplants. The quantity of meat, eggs and fish was limited to once a day (120g of meat or 200g of fish or 1 egg) Table 1. Moreover, subjects daily consumed four food supplements and liquid herbal extracts. Food supplements are high proteins (19g/portion) and very low carbohydrate (3.5g/portion) formulas simulating the aspect and taste of common carbohydrate rich foods added with dry phytoextracts (30). Liquid herbal extracts were used for their draining /toning activity, useful to reduce some commonly reported light side effects of ketogenic diets as constipation, headache and halitosis.

Outcome Measures

Primary Outcome Measures

  1. Body Weight [12 weeks]

    Body weight will be measured by an electronic scale

  2. Fat body mass [12 weeks]

    will be analysed by Dual X Ray Absorptiometry (DEXA) Hologic HorizonTM QDR RSeries Bedford, Massachusetts, USA

  3. LH [after 12 weeks]

    LH will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  4. FSH [12 weeks]

    FSH will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  5. Total testosterone [12 weeks]

    Total testosterone will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  6. Insulin [12 weeks]

    Insulin will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  7. DHEAS [12 weeks]

    DHEAS will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  8. progesterone [12 weeks]

    progesterone will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  9. estradiol [12 weeks]

    estradiol will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  10. SHBG [12 weeks]

    SHBG will be measured by immunochemiluminescent method (Roche Cobas e601, Roche Diagnostics, Mannheim, Germany)

  11. HOMA [12 weeks]

    HOMA-IR will be calculated according to the formula "insulinemia (μU/mL) x glycemia (mmol/L)/22.5

  12. blood glucose [12 weeks]

    blood glucose will be measured by enzymatic method with esokinase (Roche Cobas e702, Roche Diagnostics, Mannheim, Germany)

  13. Hirsutism . [12 weeks]

    we will use Ferriman Gallwey Score. A score of 1 to 4 is given for nine areas of the body. A total score less than 8 is considered normal, a score of 8 to 15 indicates mild hirsutism, and a score greater than 15 indicates moderate or severe hirsutism. A score of 0 indicates absence of terminal hair.

Secondary Outcome Measures

  1. Ketone bodies [12 weeks]

    Ketone bodies will be measured by Precision Xtra® Blood β-Ketone Test Strips and Precision Xtra® (28) (Abbott Laboratories, Illinois 60064-3500, USA)

  2. total cholesterol [12 weeks]

    total cholesterol will be measured by enzymatic colorimetric in homogenous phase (Roche Cobas e702, Roche Diagnostics, Mannheim, Germany)

  3. HDL cholesterol [12 weeks]

    HDL cholesterol will be measured by enzymatic colorimetric in homogenous phase (Roche Cobas e702, Roche Diagnostics, Mannheim, Germany)

  4. LDL cholesterol [12 weeks]

    LDL cholesterol will be measured by enzymatic colorimetric in homogenous phase (Roche Cobas e702, Roche Diagnostics, Mannheim, Germany)

  5. Triglycerides [12 weeks]

    TGs by an enzymatic colorimetric method (Roche Cobas e702, Roche Diagnostics, Mannheim, Germany)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:

diagnosis of PCOS according Rotterdam Criteria (at least 2 of 3 between

  • oligo/anovulation

  • hyperandrogenism

  • clinical (hirsutism or less commonly male pattern alopecia) or biochemical (raised FAI or free testosterone) polycystic ovaries on ultrasound Other inclusion criteria

  • fertile age (18-45 years);

  • BMI> 25 kg/m2,

  • desire to lose weight;

  • acceptance not to use contraceptives during the experimental period

Exclusion Criteria:
  • pregnancy and lactation,

  • hormonal therapy and/or insulin-sensitizers in the last 2 months,

  • hepatic, renal and heart diseases

Contacts and Locations

Locations

Site City State Country Postal Code
1 Nutrition and Exercise Lab, DSB, University of Padova Padova Italy 35131

Sponsors and Collaborators

  • University of Padova
  • University of Palermo
  • Universita di Verona
  • Vita-Salute San Raffaele University

Investigators

  • Principal Investigator: Antonio Paoli, MD, University of Padova

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Antonio Paoli, Professor, University of Padova
ClinicalTrials.gov Identifier:
NCT04163120
Other Study ID Numbers:
  • KDPCOS
First Posted:
Nov 14, 2019
Last Update Posted:
Nov 14, 2019
Last Verified:
Nov 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 14, 2019