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To Study the Effect of SC-FOS Prebiotics in Women With Polycystic Ovary Syndrome - Trial NCT05999097

Access comprehensive clinical trial information for NCT05999097 through Pure Global AI's free database. This phase not specified trial is sponsored by Universidad Autonoma de Chihuahua and is currently Recruiting. The study focuses on Polycystic Ovary Syndrome. Target enrollment is 40 participants.

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NCT05999097
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dietary supplement
Trial Details
ClinicalTrials.gov • NCT05999097
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To Study the Effect of SC-FOS Prebiotics in Women With Polycystic Ovary Syndrome
To Study the Clinical Effect of SC-FOS Prebiotics in Enteral Diet vs. Standard Enteral Diet on Clinical Characteristics of Patients With Polycystic Ovary Syndrome According to the Rotterdam Classification in Chihuahua, Chihuahua. A Randomized Single-Blind Clinical Trial

Study Focus

Polycystic Ovary Syndrome

Short Chain Fructooligosaccharides

Interventional

dietary supplement

Sponsor & Location

Universidad Autonoma de Chihuahua

Chihuahua, Mexico

Timeline & Enrollment

N/A

Sep 01, 2023

Sep 30, 2023

40 participants

Primary Outcome

Score of Bristol Scale,Score Short Form Health Survey (SF-36)

Summary

The purpose of this study is to determine if there is a difference in the clinical
 characteristics of patients with polycystic ovary syndrome after the administration of SC-FOS
 in the enteral diet compared to patients with a standard diet.

ICD-10 Classifications

Polycystic ovarian syndrome
Ovarian dysfunction, unspecified
Ovarian dysfunction
Other ovarian dysfunction
Neoplasm of uncertain or unknown behaviour: Ovary

Data Source

ClinicalTrials.gov

NCT05999097

Non-Device Trial