The Efficacy of Pulsed Electromagnetic Field Therapy for Management of Post-operative Pain Following Cesarean Delivery

Pain Clinical Trial

Official title:

The Efficacy of Pulsed Electromagnetic Field Therapy for Management of Post-operative Pain Following Cesarean Delivery: a Randomised, Double-blind, Placebo-controlled Study

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01383122
• Other study ID #: 11-01
• Status: Terminated
• Phase: N/A
• First received: June 24, 2011
• Last updated: March 23, 2012
• Start date: May 2011
• Est. completion date: March 2012

Study information

• Verified date: March 2012
• Source: Samuel Lunenfeld Research Institute, Mount Sinai Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Ethics Review Committee
• Study type: Interventional

Clinical Trial Summary

Pain following Cesarean delivery remains the most common post-operative complaint, and the provision of effective and safe analgesia is very important. Pain can impede the mother's ability to mobilise, and to care for and breastfeed her newborn baby.

Pulsed electromagnetic field (PEMF) devices have been used in various clinical settings, especially after plastic surgeries, to reduce postoperative swelling and pain, as well as to accelerate wound repair. PEMF therapy is simple to use, cost-effective and has no known side effects.

Despite advances in post-operative analgesia, pain relief and maternal satisfaction remain inadequate in some patients. Improving the quality of post-Cesarean analgesia while limiting undesirable side effects will enhance maternal satisfaction and reduce the risk of post-operative complications.

The investigators hypothesize that the continuous use of a PEMF device for 48 hours after Cesarean delivery will result in decreased post-operative pain scores on movement at 48 hours.

Description:

Currently, at our institution, analgesic regimens are multimodal, in that they combine analgesic drugs with differing mechanisms of action, with the aim of producing effective analgesia while minimising adverse effects. They include opioid drugs, administered both neuro-axially and systemically, as well as paracetamol and non-steroidal anti-inflammatory drugs (NSAIDs). Opioids, while effective, have significant adverse effects, including sedation, nausea, vomiting and constipation. Non-steroidal anti-inflammatory drugs (NSAIDs) can reduce opioid consumption, but also have side effects, and are contra-indicated in a significant number of patients. Therefore there remains considerable scope to improve post-Cesarean analgesia.

Pulsed electromagnetic field (PEMF) technology relieves edema, inflammation and pain by stabilizing leaking cell membranes. The short bursts of electrical current do not produce heat or interfere with nerve or muscle function. The pulsed energy drives out edematous fluid along with by-products of the damaged tissue, which reduces swelling and helps re-establish cell-cell communication. The device is easily applied over the wound dressing, and has no known side effects for either the mother or the infant.

As the rate of Cesarean delivery continues to increase, and there remain significant problems with current analgesic regimens, the use of pulsed electromagnetic field therapy has the potential to considerably improve acute and chronic post-Cesarean pain management, and lead to a widespread change in clinical practice.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 125
• Est. completion date: March 2012
• Est. primary completion date: January 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• 18 years or older

• full term singleton pregnancy

• undergoing elective cesarean delivery

Exclusion Criteria:

• Patients who have refused, are unable to give or have withdrawn consent

• Patients unable to communicate fluently in English

• Patients with American Society of Anesthesiologists (ASA) classification of 3 or greater

• Patients with chronic pain, or neuropathic analgesic drugs

• Patients in use of antidepressant and psychotropic drugs

• Patients with a history of opioid or intravenous drug abuse

• Patients with known allergy or contra-indication to any other drugs used in this trial

• Patients who have refused spinal anesthesia, or those in whom it is contra-indicated

• Patients with a history of previous cesarean delivery and persistent pain

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Pain
• Pain, Postoperative

Intervention

Device:
• Pulsed electromagnetic field device (ActiPatch TM)
Wire loop of pulsed electromagnetic field device is taped around the wound for 48 hours.
• Inactive pulsed electromagnetic field device (ActiPatch TM)
Wire loop of pulsed electromagnetic field device is taped around the wound for 48 hours.

Locations

Country	Name	City	State
Canada	Mount Sinai Hospital	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
Samuel Lunenfeld Research Institute, Mount Sinai Hospital

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain score by visual analogue scale (VAS) on movement at 48 hours postoperatively		48 hours	No
Secondary	Pain at rest and on movement by VAS, and maternal satisfaction at 24 & 48 hours postoperatively		48 hours	No
Secondary	Opioid consumption at 24 & 48 hours postoperatively		48 hours	No
Secondary	Assessment of side effects: nausea, vomiting, sedation & itchiness		48 hours	No
Secondary	Presence of pain 6 weeks postoperatively		6 weeks	No