PENS or TENS for Pain in Pancreatic Cancer
Percutaneous Electrical Nerve Stimulation or Transcutaneous Electrical Nerve Stimulation for Pain in Patients With Pancreatic Cancer
1 other identifier
interventional
36
1 country
1
Brief Summary
This study evaluates the effect of percutaneous electrical nerve stimulation (PENS) and transcutaneous nerve stimulation (TENS) for pain relieving in patients with pancreatic cancer. Patients will randomly allocated into PENS group, Tens group and control group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable pain
Started Oct 2017
Typical duration for not_applicable pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 27, 2017
CompletedFirst Submitted
Initial submission to the registry
October 28, 2017
CompletedFirst Posted
Study publicly available on registry
November 6, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 26, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
August 26, 2019
CompletedSeptember 12, 2019
October 1, 2018
6 months
October 28, 2017
September 10, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
visal analogue scale (VAS) score
VAS score before,during and 3 days after treatment
D0-D6
Secondary Outcomes (2)
quantity of analgesic medication
D0-D6
times of breakthrough pain (BTP)
D0-D6
Other Outcomes (1)
complications
D1-D2
Study Arms (3)
percutaneous stimulation
EXPERIMENTALPENS in 2/100HZ, 30 min for each time, twice a day, for 3 days. With conventional analgesic medication if necessary.
trancutaneous stimulation
EXPERIMENTALTENS in 2/100HZ, 30 min for each time, twice a day, for 3 days. With conventional analgesic medication if necessary.
Control
NO INTERVENTIONConventional analgesic medication is offered.
Interventions
Eligibility Criteria
You may qualify if:
- Pancreatic cancer with pain;
- Haven't underwent neurolytic celiac plexus block in the past 1 month;
- With anticipatory survival of more than 3 months.
You may not qualify if:
- Metastatic pancreatic cancer;
- Can not tolerate 30 min of lieing in prostrate or side position;
- PS\>3;
- Who has been recruited in other clinical trial for pain releiving;
- Who underwent radiotherapy or local radiactive seeds implantation for pain releiving in the past month;
- Imaging diagnosed with encephalic tumor or metastasis;
- Who with cardiac pacemaker or metal stand;
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fuda Cancer Hospital
Guangzhou, Guangdong, 510665, China
Related Publications (5)
Hurlow A, Bennett MI, Robb KA, Johnson MI, Simpson KH, Oxberry SG. Transcutaneous electric nerve stimulation (TENS) for cancer pain in adults. Cochrane Database Syst Rev. 2012 Mar 14;2012(3):CD006276. doi: 10.1002/14651858.CD006276.pub3.
PMID: 22419313RESULTPeng L, Min S, Zejun Z, Wei K, Bennett MI. Spinal cord stimulation for cancer-related pain in adults. Cochrane Database Syst Rev. 2015 Jun 29;2015(6):CD009389. doi: 10.1002/14651858.CD009389.pub3.
PMID: 26121600RESULTChen H, Liu TY, Kuai L, Zhu J, Wu CJ, Liu LM. Electroacupuncture treatment for pancreatic cancer pain: a randomized controlled trial. Pancreatology. 2013 Nov-Dec;13(6):594-7. doi: 10.1016/j.pan.2013.10.007. Epub 2013 Oct 23.
PMID: 24280575RESULTPaley CA, Johnson MI, Tashani OA, Bagnall AM. Acupuncture for cancer pain in adults. Cochrane Database Syst Rev. 2015 Oct 15;2015(10):CD007753. doi: 10.1002/14651858.CD007753.pub3.
PMID: 26468973RESULTHe L, Tan K, Lin X, Yi H, Wang X, Zhang J, Lin J, Lin L. Multicenter, randomized, double-blind, controlled trial of transcutaneous electrical nerve stimulation for pancreatic cancer related pain. Medicine (Baltimore). 2021 Feb 5;100(5):e23748. doi: 10.1097/MD.0000000000023748.
PMID: 33592831DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Lizhi Niu, Dr.
Fuda Cancer Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Participant is allocated randomly by staff A, and grouping situation is concealed; Technician (stuff B) or chargeing docotor operates PENS or TENS, or administers oral analgesic medication; Related datas are collected according to perdetermined forms by stuff C; Outcomes are assessed by stuff D.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 28, 2017
First Posted
November 6, 2017
Study Start
October 27, 2017
Primary Completion
April 26, 2018
Study Completion
August 26, 2019
Last Updated
September 12, 2019
Record last verified: 2018-10