Hand-foot Syndrome

2

Review clinical trials related to Hand-foot Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

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

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.

Participants needed: 220
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Qinghai UniversityUpdated: Dec 12, 2024Locations: 1
Eligibility criteria

Sign a written informed consent form; [+7]

Previous use of capecitabine or liposome doxorubicin or any other tyrosine kinas... [+10]

Status: Recruiting

Photobiomodulation Therapy in the Management of Hand-foot Syndrome and Hand-foot Skin Reaction

Hand-foot syndrome (HFS) is a side effect of chemotherapy. HFS is characterized by redness, swelling, and pain on the palms of the hands and/or soles of the feet, which can progress to blistering. Hand-foot skin reaction (HFSR) refers to symptoms affecting the hands and/or feet associated with multikinase inhibitors (TKIs). HFS and HFSR are painful complications that can lead to compromised daily activities, sleep-wake disturbance and impaired mobility, eventually decreasing Quality of Life (QoL). Photobiomodulation therapy (PBMT) is a non-invasive therapy based on the application of visible and/or near-infrared light produced by a laser diode or a light-emitting diode. The scientifically proven biologic effects of PBM are improved wound healing, and a reduction in pain, inflammation, and oedema. The aim of this study is to evaluate the effectiveness of PBMT in the management of HFS and HFSR.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Jessa HospitalUpdated: Jun 18, 2023Locations: 2
Eligibility criteria

Diagnosed with cancer of different aetiologies [+5]

Pre-existing skin rash, ulceration or open wound in the treatment area (hand, fo... [+3]