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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02510066
Other study ID # 12401905600
Secondary ID
Status Recruiting
Phase Phase 3
First received July 23, 2015
Last updated July 27, 2015
Start date July 2015
Est. completion date June 2017

Study information

Verified date July 2015
Source Shanghai Cancer Hospital, China
Contact Hao Chen
Phone 86-13601996751
Email chengkll@sina.com
Is FDA regulated No
Health authority China: Science and Technology Commission of Shanghai Municipality
Study type Interventional

Clinical Trial Summary

This study compares the effect of acupuncture and placebo acupuncture on advanced pancreatic cancer pain and then investigates its potential mechanism of peripheral blood.


Description:

Acupuncture may alleviate abdominal or back pain of patients with advanced pancreatic cancer. Acupuncture participants would receive electroacupuncture on Jiaji (Ex-B2) points for 3 times in a week. Placebo acupuncture participants would receive placebo acupuncture on non-point points for the same period. Pain scores on numeric rating scale (NRS) and blood levels of β-endorphin and nerve growth factor are compared.


Recruitment information / eligibility

Status Recruiting
Enrollment 62
Est. completion date June 2017
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Advanced pancreatic cancer at ?-? stage diagnosed by histological/cytological examination.

- Pain score of abdominal or back pain =3 on a numeric rating scale (NRS) graduated from 0 to 10.

- Stable dose of analgesics at least 72 hours before randomization.

- Expected survival time more than 1 month.

Exclusion Criteria:

- Another cause for abdominal or back pain (such as prolapse of lumbar intervertebral disc, ulcer or other intra-abdominal disorder).

- Acupuncture treatment in the past.

- Contraindications for the use of acupuncture (such as severe allergies, bleeding tendency, infectious dermatosis and ulcer or scar at points).

- Unable to give informed consent.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Acupuncture
Disposable stainless steel filiform needles (40mm in length and 0.30mm in diameter) are inserted perpendicularly into T8-T12 Jiaji (Ex-B2) points bilaterally to a depth of 25 mm. After De Qi sensation is achieved, the handles of needles on homolateral T8 and T12 Jiaji are respectively connected to the Han's acupoint nerve stimulator at a frequency of 2/100 Hz and a current of 1mA with a disperse-dense waveform for 30 minutes.
Placebo acupuncture
Placebo acupuncture needles (Dongbang AcuPrime Acupuncture Inc., South Korea) are used on the non-point points at the same level as T8 and T12 Jiaji, 4.5 cun lateral to the posterior median line. The needles with blunt tips are quickly put onto points without inserting into the skin. The needles on homolateral points at the same level as T8 and T12 Jiaji are then connected to the electric stimulator, but with zero frequency and electric current.

Locations

Country Name City State
China Shanghai Cancer Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Cancer Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain scores, assessed with numeric rating scale (NRS) 1 week No
Secondary Karnofsky performance status (KPS) score 1 week No
Secondary Blood levels of ß-endorphin 1 week No
Secondary Blood levels of nerve growth factor 1 week No
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