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Observational Study to Evaluate the Quality of Life of Healthy Postmenopausal Women Who Take Coenzyme Q-Ubiquinol

Observational Study With Food Product to Evaluate the Quality of Life of Healthy Postmenopausal Women Who Take Coenzyme Q-Ubiquinol, Compared With Another Group of the Same Age That Does Not Take coenzymeQ-Ubiquinol

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03429231
Enrollment
40
Registered
2018-02-12
Start date
2017-11-23
Completion date
2018-04-15
Last updated
2018-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Status

Brief summary

Observational study about quality of life in postmenopausal women taking coenzyme Q compared to another group of women of the same age who do not take it

Detailed description

Observational study to evaluate the subjective assessment performed by healthy postmenopausal women who are taking coenzyme Q for 3 months, compared with other groups of the same characteristics that do not take it

Interventions

DIETARY_SUPPLEMENTCoenzima Q - QubiquinolCoenzyme Q - Qubiquinol

Patients in the active group will take one tablet a day orally

Sponsors

Dr. Santiago Palacios
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Inclusion criteria

* Postmenopausal woman between 45 and 65 years old * Woman who is taking coenzyme Q-Ubiquinol and who will continue taking at least the next 3 months * Woman not taking Coenzyme Q-Ubiquinol and not going to take it in the next 3 months Exclusión Criteria: * Patients with severe mental illness. * Suspicion or abuse of alcohol or other drugs during the 12 months prior to the selection * Any other consideration or finding that, in the opinion of the investigator, considers the non-participation of the subject in the study.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Quality of Life at 3 monthsBaseline and 3 monthsTo evaluate the quality of life in healthy postmenopausal women who are taking Coenzyme Q-Ubiquinol for 3 months in comparison with another group that does not take them. The Cervantes Health-Related Quality of Life scale for menopause will be used for this outcome. In that scale next to the 0 and the 5 there are words that describe two opposite answers to the question. Between the 0 and the 5 there are also four boxes numbered 1 to 4. The participants should answer the questions by checking the box that best represents what they think and feel. In other words, they should check 5 if they are completely agree and 0 they are completely disagree. If they are not completely agree or disagree, they should check the boxes in between

Secondary

MeasureTime frameDescription
Change from Baseline General Health at 3 monthsBaseline and 3 monthsHealth Scale Euroqol EQ-5D will be used for this outcome
Change from Baseline Mood at three monthsBaseline and 3 monthsAn analogic scale will be used for this outcome in wich 0 points is the best mood and 10 points is worst mood
Change from Baseline Cramps at three monthsBaseline and 3 monthsTo assess changes in cramps in patients who had them, a general questionnaire about Cramps will be used to assess mainly the intensity and frequency of crambs. Regarding the intensity 0 is the lower pain and 10 is the worst pain

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026