Clinical trial Recruiting at 1 site Observational Ages 18 and up

Guaraná Supplement for Cancer-Related Fatigue in People Undergoing Treatment

Official title: Evaluation of the Effectiveness of Guaraná (Paullinia Cupana) Supplementation in Reducing Cancer-Related Chronic Fatigue

Run by Centro de Tratamiento e Investigación sobre Cáncer, Luis Carlos Sarmiento Angulo · NCT07816263 · Data updated 2026-11-12

This study tests whether taking guaraná capsules helps reduce cancer-related fatigue and improve quality of life in adults with breast, lung, colorectal, or gastric cancer who are actively receiving treatment.

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Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorCentro de Tratamiento e Investigación sobre Cáncer, Luis Carlos Sarmiento Angulo
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Bogotá, Bogota D.C.)
StatusRecruiting
StartedJune 20, 2026
Main results expectedJanuary 18, 2027
Study endsJune 20, 2027
Registry record updatedSeptember 11, 2026
Trial IDNCT07816263 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults with breast, lung, colorectal, or gastric cancer receiving active systemic therapy who have completed at least three cycles of chemotherapy.

Probably not a fit

Patients unlikely to benefit may include those who are intolerant to caffeine or methylxanthines, have uncontrolled cardiovascular disease, or are on CNS stimulants or anticoagulant therapy.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pragmatic, prospective study observes the effects of guaraná supplementation on fatigue and quality of life in patients undergoing cancer treatment. Participants take 50 mg of guaraná twice daily for up to six 21-day cycles, with assessments at baseline, week 3, and end of treatment. Primary outcome is change in fatigue using FACIT-F and BFI; secondary outcomes include quality of life (EORTC QLQ-C30), adverse events, and caregiver-perceived quality of life. A subset of 30 participants will have exploratory measurements of inflammatory markers and adherence data collected.

Why it matters

Potential benefit: If successful, guaraná could offer a simple, tolerable option to lessen fatigue and possibly improve daily functioning for patients during treatment.

How similar studies have gone: Prior small studies and meta-analyses have suggested fatigue benefits from guaraná but results are inconsistent, and rigorous evidence is still needed.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Histologic diagnosis of breast, lung, colorectal, cervical or gastric cancer
* Receiving active cancer treatment
* Has completed at least three cycles of chemotherapy

Exclusion Criteria:

* Intolerance to the oral route
* Contraindications to guaraná intake
* Uncontrolled cardiovascular disease (uncontrolled atrial fibrillation, symptomatic tachyarrhythmias, prolonged QT)
* History of intolerance to caffeine, methylxanthines, or flavonoids
* Use of CNS stimulants
* Recent history of bleeding
* Use of warfarin or any other vitamin K antagonist
* Use of theophylline

Where it's running

  • Fundación CTIC Centro de Tratamiento e Investigación sobre Cáncer Luis Carlos Sarmiento Angulo
    Bogotá, Bogota D.C., Colombia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.