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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03626220
Other study ID # CMUH106-REC2-117
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 27, 2018
Est. completion date October 10, 2020

Study information

Verified date August 2019
Source China Medical University Hospital
Contact Chien-Chen Huang(Attending physician), master
Phone (06)355-3111
Email chenchinh2013@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Peripheral neuropathy is currently the second most common side effect after chemotherapy, second only to the side effects of blood toxicity. A variety of chemotherapy drugs may induce peripheral neurotoxicity, and cause by the cumulative dose of chemotherapy drugs. Symptoms include sensory parasthesia, feeling dull or numbness, glove-like feeling distributed in the palm. The currently most effective way is to interrupt the treatment or adjust the dose of chemotherapeutic drugs, but it is easy to make patients discontinue chemotherapy. The purpose of this study is to explore the impact of acupuncture on neurological symptoms and quality of life. Three kinds of questionnairs will be used:(1) Brief pain inventory- short form to assess the extent of pain, and the impact of daily life. (2) FACT/GOG-NTX-13 (Version 4) to assess changes in neurological symptoms; (3) WHOQOL-BREF to assess changes in the quality of life of patients. The course of treatment was evaluated for nine weeks. Changes in neurological function and quality of life will be evaluated before treatment, the third week of treatment, the sixth week of treatment, till the ninth week. The aim of this study is to confirm that acupuncture can improve peripheral neuropathy after chemotherapy, in order to enhance breast cancer patients' quality of life, and provide the new opportunity for integrative therapy between Chinese and Western medicine.

Keywords:acupuncture , chemotherapy-induced peripheral neuropathy


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date October 10, 2020
Est. primary completion date October 10, 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- more than 20 yeas old Female

- TypeI-IV breast cancer patients

- complete chemotherapy

- chemotherapeutic agents include taxanes?platinum compounds ect

- ECOG<3

- NCI common terminology criteria for adverse events,v4.0: more than grade1 ?

Exclusion Criteria:

- average life expectancy<3months

- diabetic neuropathy

- inflammatory neuropathy

- metabolic neuropathy

- severe blood coagulopathy or bleeding tendency

- unstable heart disease

- neuro-muscular disease

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
acupuncture
manually manipulate acupuncture at CV6 and three acupoints on each arms and legs

Locations

Country Name City State
Taiwan An Nan Hospital,China Medical University Tainan

Sponsors (1)

Lead Sponsor Collaborator
China Medical University Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (1)

Greenlee H, Crew KD, Capodice J, Awad D, Buono D, Shi Z, Jeffres A, Wyse S, Whitman W, Trivedi MS, Kalinsky K, Hershman DL. Randomized sham-controlled pilot trial of weekly electro-acupuncture for the prevention of taxane-induced peripheral neuropathy in — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary FACT/GOG-NTX-13 (Version 4) Prorated subscale score = [Sum of item scores] x [N of items in subscale]÷ [N of items answered] For all FACIT scales and symptom indices, the higher the score the better the QOL. 4 times in 9 weeks
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