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NCT06602167

Electroacupuncture Combined With Self-administered Acupressure for the Prevention of Capecitabine-Associated Hand-Foot Syndrome

Recruiting now NA Last updated 12 December 2024
What this trial tests

NA trial testing True electroacupuncture + True self-administered acupressure in Capecitabine in 220 participants. Currently enrolling.

Timeline
8 October 2024
Primary endpoint
30 July 2027
31 December 2027

Quick facts

Lead sponsorAffiliated Hospital of Qinghai University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposeprevention
Enrollment220
Start date8 October 2024
Primary completion30 July 2027
Estimated completion31 December 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Affiliated Hospital of Qinghai University

Who can join

Adults 18 to 85, any sex, with Capecitabine or Hand-foot Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study hypothesizes that electroacupuncture combined with self-administered acupressure plus doctor-prescribed treatment is effective in preventing Hand-Foot Syndrome (HFS) caused by capecitabine. It aims to explore the effectiveness of this combined approach in preventing HFS in patients with malignant tumors undergoing oral capecitabine treatment. Further exploration of prevention and treatment methods may enhance the quality of life for patients during the treatment process.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Capecitabine

Currently open trials in the same condition.

Other Affiliated Hospital of Qinghai University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06602167.

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