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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01184963
Other study ID # 04-364
Secondary ID
Status Completed
Phase N/A
First received August 17, 2010
Last updated August 18, 2010
Start date March 2008
Est. completion date December 2009

Study information

Verified date December 2009
Source Federal University of Rio Grande do Sul
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

The objective of this study is to assess the effects of a high protein (HP) and a normal protein diet (NP) on patients with polycystic ovary syndrome (PCOS) and body mass index (BMI)-matched controls in a sample of southern Brazilian women.

Patients will be randomized to receive high protein (30% protein, 40% carbohydrate, 30% lipid) or normal protein (15% protein, 55% carbohydrate, 30% lipid) during eight weeks.

The investigators hypothesis is that a different diet composition may have influences in changes of the main characteristics of PCOS, like hyperandrogenism and metabolic syndrome.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 2009
Est. primary completion date September 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 14 Years to 35 Years
Eligibility Inclusion Criteria:

- women of reproductive age

- BMI ranging from 18.5 to 39.9 kg/m²

Exclusion Criteria:

- Use of any drugs known to interfere with hormone levels for at least 3 months before the study

- Women with known type 2 diabetes, liver or renal disease or thyroid dysfunction

- Other hyperandrogenic disorders than PCOS

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
High protein diet
High protein diet (30% protein, 40% carbohydrate, 30% lipid)
Normal protein diet
Normal protein diet (15% protein, 55% carbohydrate, 30% lipid

Locations

Country Name City State
Brazil Hospital de Clínicas de Porto Alegre Porto Alegre Rio Grande do Sul

Sponsors (4)

Lead Sponsor Collaborator
Federal University of Rio Grande do Sul Conselho Nacional de Desenvolvimento Científico e Tecnológico, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Hospital de Clinicas de Porto Alegre

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in corporal weight 8 weeks No
Secondary Changes in body composition 8 weeks No
Secondary changes in hormone and metabolic profile. 8 weeks No
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