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Acupoint Electric Stimulation Combined With Tropisetron in Preventing and Treating Nausea and Vomiting After TACE

Acupoint Electric Stimulation Combined With Tropisetron in Preventing and Treating Nausea and Vomiting After TACE

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01895010
Enrollment
74
Registered
2013-07-10
Start date
2013-06-30
Completion date
2014-12-31
Last updated
2013-07-10

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

Conditions

Nausea, Vomiting, Metastatic Liver Cancer

Keywords

prevention and treatment, improvement of the patient's appetite, TACE

Brief summary

Observation on acupoint electric stimulation combined with tropisetron in preventing and treating nausea and vomiting and improving the patient's appetite after TACE for primary or metastatic liver cancer patients.

Detailed description

* Classification of nausea and vomiting, as measured by NCI CTC-AE version 3 * The improvement of appetite, as measure by the classification of Appetite in accordance with NCI CTC-AE version 3. * Quality of life: use M. D. Anderson symptom scale (the m. d. Anderson Symptom Inventory,MDASI)

Interventions

DEVICEacupoint electric stimulation

acupoint electric stimulation combined with tropisetron 6mg before TACE

only tropisetron 6mg before TACE

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ECOG physical status 0,1,2 * would accept the transcatheter hepatic arterial chemoembolization of primary or metastatic liver cancer patients; * Adult male and female 3, age 18 years old; * the chem-scheme of arterial infusion chemotherapy based on oxaliplatin dosage of 200mg; * signed the informed consent and understand the study design; * Organ function examination in patients must meet the following laboratory indexes: Neutrophil\>500/Ul, hemoglobin \> 8 gm/dL, platelet \>100000/uL,Creatinine \< 2 mg/dL bilirubin \< 1.5 mg/dL, , alanine aminotransferase \< 3 times the normal value, albumin \>30g/L * understand and complete quality of life scale ; * women of childbearing age urine pregnancy test was negative.

Exclusion criteria

* The combined use of other venous chemotherapy within 5 days after TACE; * skin infection on or near the points; * skin hyperalgesia, unable to withstand electrical stimulation; * other confounding factors may cause nausea and vomiting (such as intestinal obstruction, anorexia, etc.); * heart, cerebrovascular accident history or the history of spinal cord injury; * intestinal obstruction lead to nausea and vomiting * installing pacemaker; * cognitive dysfunction, unable to finish Scale; * currently using acupuncture therapy.

Design outcomes

Primary

MeasureTime frame
Classification of nausea and vomiting12 month

Secondary

MeasureTime frame
The improvement of appetite12 month

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026