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The Prevalence of Chronic Pain and Continued Opioid Use After Cardiac Surgery

The Prevalence of Chronic Pain and Continued Opioid Use After Cardiac

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03412448
Acronym
Doul-Card
Enrollment
320
Registered
2018-01-26
Start date
2017-06-01
Completion date
2018-08-01
Last updated
2018-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgery, Chronic Pain, Opioid Use

Keywords

chronic pain, cardiac surgery, opioids

Brief summary

The authors propose to evaluate the prevalence of chronic post-operative pain (CPOP) and continued opioid use in the population that has undergone cardiac surgery at the Montreal Heart Institute. In addition, the authors wish to evaluate the presence of known risk factors for CPOP in this population.

Detailed description

This study will use a 15-minute telephone survey to prospectively evaluate the prevalence and intensity of chronic pain 6 months and 1 year after cardiac surgery. Data on the level of post-operative pain experienced on days 1 to 4, at the time of surgery, as well as opioid consumption, adjuvant pain treatments and other variables of interest that are currently recorded prospectively at time of surgery will be culled from patient charts. Additionally, the possibility of continued opioid use by patients at 6 months post-surgery will be evaluated.

Interventions

OTHERobservation

Observation,

Sponsors

Montreal Heart Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All patients who have surgery at the Montreal Heart Institute between October 1 2017 and October 1 2018 will be eligible for selection.

Exclusion criteria

Patients who have declined to be contacted after surgery as noted on the MHI form Consent for futur projects. All patients who accepted to be contacted but decline to participate when contacted after their surgery. Patients who cannot be reached by phone. Patients who cannot speak French

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of CPOP6 (+ or - two weeks) months after surgeryPrevalence of CPOP at 6-months post-surgery.

Countries

Canada

Contacts

Primary ContactJennifer Cogan, MD
cogan.jennifer@me.com514-376-3330
Backup ContactMichelle Plante, PhD
michele.plante@icm-mhi.org514-37603330

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026