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Enrolling By InvitationNCT06054802

Perioperative Sleep Quality and Postoperative Pain Outcomes

The Influence of Perioperative Sleep Quality on Postoperative Pain Outcomes in Pediatric Patients Undergoing Knee Surgery

Status
Enrolling By Invitation
Phase
Study type
Observational
Enrollment
166 (estimated)
Sponsor
Grant Heydinger · Academic / Other
Sex
All
Age
10 Years – 18 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, observational cohort study that will examine how sleep quality impacts postoperative pain and opioid consumption for pediatric patients. The investigators will administer a questionnaire preoperatively to determine which patients have poor or good sleep quality. They will then compare postoperative pain and opioid use between groups for two weeks following surgery. For a secondary aim, investigators will use electronic medication vials (eCAP) to monitor participants' medication use at home and compare to self-reporting.

Conditions

Interventions

TypeNameDescription
DEVICEeCAPeCap™ has the look and feel of a regular prescription bottle and records real-time adherence data, tracking each opening with the date and time.

Timeline

Start date
2025-02-03
Primary completion
2027-12-01
Completion
2027-12-01
First posted
2023-09-26
Last updated
2026-04-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06054802. Inclusion in this directory is not an endorsement.

Perioperative Sleep Quality and Postoperative Pain Outcomes (NCT06054802) · Clinical Trials Directory