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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06064838
Other study ID # FLALOC
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2023
Est. completion date December 31, 2024

Study information

Verified date September 2023
Source National Polytechnic Institute, Mexico
Contact Munguia, MD, PhD
Phone 54471424
Email investigacion.issste19@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study use a triple blind, placebo-controlled design enrolling male and female subjects between 30-70 yo to evaluate the effect of daily consumption of a cacao supplement on inflammation, endothelial damage, handgrip strenght, fatigue scale and quality of life.


Description:

The study use a triple blind, placebo-controlled design enrolling male and female subjects between 30-70 yo distributed homogeneously at random in two groups: the control group (Placebo) and the intervention group (Cacao Flavonoids) both groups affected for 90 days. The variables to consider will be: Interleukins (IL-1b, IL-6), Tumoral Necrosis Factor alpha (TNF-α) and syndecan-1. For physical performance is evaluated the handgrip strength. The investigators also assessed quality of life using the Health Related QoL (EQ-5D) questionnaire, and the numerical fatigue rating scale.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 31, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers No
Gender All
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria: - Post-COVID-19 patients, at least 6 months after symptom onset - Chronic fatigue Exclusion Criteria: - Allergy or intolerance caused by active ingredients - Pregnancy or lactation - BMI >35 - chronic liver disease - chronic kidney disease

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Flavonoids
1 capsule every 12h for 90 days

Locations

Country Name City State
Mexico C.E. Indianilla Mexico City

Sponsors (2)

Lead Sponsor Collaborator
Guillermo Ceballos Reyes Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Interleukin-1b Plasmatic concentration At 0 and 90 day
Primary Interleukin-6 Plasmatic concentration At 0 and 90 day
Primary TNF-alpha Plasmatic concentration At 0 and 90 day
Primary Syndecan-1 Plasmatic concentration At 0 and 90 day
Secondary EQ-5D questionnaire Self-administered health index that explores five domains At 0 and 90 day
Secondary Analog Visual Scale Use of a Analog Visual Scale to measure the quality of life, graded 0 (worst) to 100 (best) for the perception of wellbeing. At 0 and 90 day
Secondary Numerical fatigue rating scale fatigue rating scale graded 0 (best) to 100 (worst) At 0 and 90 day
Secondary Handgrip strength Measures static force in kilograms that the hand can squeeze around a dynamometer At 0 and 90 day
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