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Perioperative Sleep Quality and Postoperative Pain Outcomes

NCT06054802 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 166

Last updated 2026-04-06

No results posted yet for this study

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

  • Surgery
  • Pain
  • Sleep
  • Spinal Fusion

Interventions

DEVICE

eCAP

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

Sponsors & Collaborators

  • Grant Heydinger

    lead OTHER

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-03
Primary Completion
2027-12-31
Completion
2027-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06054802 on ClinicalTrials.gov