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A study of how transcutaneous electrical nerve stimulation can be used to decrease pain in patients who have undergone a sternotomy incisio

Not Applicable
Conditions
Pain in post-sternotomy patients
Surgery
Registration Number
ISRCTN12394749
Lead Sponsor
niversity of Malta
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
90
Inclusion Criteria

1. Patients above the age of 18 years
2. Both male and female patients
3. Elective cardiac surgery via longitudinal median sternotomy
4. Consenting to participate in the study

Exclusion Criteria

1. Previous history of chronic pain, drug or alcohol abuse
2. Pre-operative use of narcotics (except for standard protocol pre-operative morphine administered prior to the surgery in question)
3. Pre-operative use of TENS
4. Pre-operative shoulder pain or decrease in shoulder ROM
5. Cancer or metastatic disease
6. Patients with a pacemaker
7. Pregnancy
8. Epilepsy
9. Surgeon reported cognitive impairments
10. Previous sternotomy procedures
11. Other types of incisions different from sternotomies
12. Prolonged mechanical ventilation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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