Clinical trials

5

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Electroacupuncture for Preventing Chemotherapy-Induced Peripheral Neuropathy in Patients With Early-stage Cancer

This randomized controlled clinical trial aims to clarify the clinical efficacy and safety of electroacupuncture combined with thumbtack needle for the prevention of chemotherapy-induced peripheral neuropathy(CIPN), and to provide high-level evidence-based medicine for the prevention of CIPN in patients with early stage cancer. At the same time, the effects of electroacupuncture on the median nerve, tibial nerve, sural nerve sensory conduction velocity and sensory nerve action potential, as well as on the median nerve and tibial nerve motor conduction velocity will be analyzed.

Participants needed: 278
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Qinghai UniversityUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+7]

Patients with advanced cancer. [+9]

Status: Not yet recruiting

Electroacupuncture for Preventing Chemotherapy-Induced Peripheral Neuropathy in Patients With Advanced Cancer

This randomized controlled clinical trial aims to clarify the clinical efficacy and safety of electroacupuncture combined with thumbtack needle for the prevention of chemotherapy-induced peripheral neuropathy(CIPN), and to provide high-level evidence-based medicine for the prevention of CIPN in patients with advanced cancer. At the same time, the effects of electroacupuncture on the median nerve, tibial nerve, sural nerve sensory conduction velocity and sensory nerve action potential, as well as on the median nerve and tibial nerve motor conduction velocity will be analyzed.

Participants needed: 264
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Qinghai UniversityUpdated: Jun 12, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+7]

Patients with early-stage cancer. [+9]

Status: Recruiting

Olanzapine Plus Metoclopramide for the Prevention of Opioid-Induced Nausea and Vomiting

The goal of this clinical trial is to evaluate the efficacy and safety of olanzapine plus metoclopramide in preventing opioid-induced nausea and vomiting (OINV) in adult patients with advanced cancer who are initiating strong opioid therapy. The main questions it aims to answer are: (1) Does the combination of olanzapine and metoclopramide reduce the incidence of OINV? (2)What adverse events do participants experience when taking the combination of olanzapine and metoclopramide? Researchers will compare the olanzapine-metoclopramide combination to a no prophylactic treatment control group to determine whether the combination is effective in preventing OINV. Participants will: Take olanzapine (2.5 mg/day ) and metoclopramide (10 mg three times daily) or receive no prophylaxis for 7 days; Through follow-up, nausea, vomiting, the time of the first attack of nausea and vomiting, the duration of nausea and vomiting, the use of strong opioids and adverse events were evaluated and recorded, as well as the pain score (using NRS) and quality of life (EQ-5D-5L) of the patients were evaluated at baseline and on day 7.

Participants needed: 222
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Qinghai UniversityUpdated: Apr 27, 2026Locations: 1
Eligibility criteria

Patients with malignant tumors diagnosed by pathology or histology; [+10]

Diabetic patients with a clear diagnosis and poorly controlled blood sugar level... [+11]

Status: Recruiting

Electroacupuncture Treatment of Peripheral Neuropathy After Taxane Chemotherapy for Breast Cancer

Electroacupuncture treatment of peripheral neuropathy after taxane chemotherapy for breast cancer

Participants needed: 162
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Affiliated Hospital of Qinghai UniversityUpdated: Jan 14, 2025Locations: 1
Eligibility criteria

Breast cancer patients diagnosed by pathology; [+3]

Non breast cancer patients; [+4]

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]