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Recruiting INTERVENTIONAL NCT02352116

Evaluation of Post-PACU Pain Management in Pediatric Surgery

Evaluation of Post-PACU Pain Management Experiences in Pediatric Ambulatory Surgery Patients

Sponsor: Columbia University

Conditions Pain
Updated 13 times since 2017 Last updated: Apr 20, 2026 Started: Jun 1, 2013 Primary completion: Dec 1, 2027 Completion: Dec 1, 2027
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT02352116, this observational or N/A phase trial focuses on Pain and remains actively recruiting participants. Sponsored by Columbia University, it has been updated 13 times since 2013, reflecting substantial change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

Study Description(click to expand)

With the increased frequency and popularity of pediatric ambulatory surgery, there is a greater need for evaluation of the postoperative pain experience after discharge from the hospital. Pain is one of the most significant factors affecting the postoperative experience in adults, and also be true in the pediatric population. Control of postoperative pain in children after discharge from the hospital poses particular challenges due to dependence on parental or caretaker ability to properly evaluate the child's pain, their understanding of appropriate dosing of pain medications, and their willingness to administer enough medications until sufficient relief is achieved. The investigators aim to assess the differences in reported pain between groups who receive additional face-to-face education versus the current standard of care at a major US teaching hospital. The study will assess pain management after surgery using parental reports and questionnaires to assess their child's pain at multiple time points during the study. Additionally, this study will also assess baseline behavioral attributes of children and will compare behavioral changes at 24-48 hours, 7-10 days, and 2-4 weeks postoperatively as these behavior changes may also affect overall postoperative experience. This study is divided into phase I and phase II. Phase I is the...

With the increased frequency and popularity of pediatric ambulatory surgery, there is a greater need for evaluation of the postoperative pain experience after discharge from the hospital. Pain is one of the most significant factors affecting the postoperative experience in adults, and also be true in the pediatric population. Control of postoperative pain in children after discharge from the hospital poses particular challenges due to dependence on parental or caretaker ability to properly evaluate the child's pain, their understanding of appropriate dosing of pain medications, and their willingness to administer enough medications until sufficient relief is achieved.

The investigators aim to assess the differences in reported pain between groups who receive additional face-to-face education versus the current standard of care at a major US teaching hospital. The study will assess pain management after surgery using parental reports and questionnaires to assess their child's pain at multiple time points during the study. Additionally, this study will also assess baseline behavioral attributes of children and will compare behavioral changes at 24-48 hours, 7-10 days, and 2-4 weeks postoperatively as these behavior changes may also affect overall postoperative experience.

This study is divided into phase I and phase II. Phase I is the initial assessment of the investigators' institution's pain management in healthy pediatric patients undergoing ambulatory surgical procedures. Phase II consists of randomized trial which includes a randomized intervention group and control group. The group selected randomly for intervention will receive additional teaching regarding what to expect in terms of postoperative pain and how to properly identify pain in children.

Status Flow

~Jan 2017 – ~Jun 2018 · 17 months · monthly snapshot~Jun 2018 – ~Feb 2019 · 8 months · monthly snapshot~Feb 2019 – ~Aug 2020 · 18 months · monthly snapshot~Aug 2020 – ~Jan 2021 · 5 months · monthly snapshot~Jan 2021 – ~Sep 2021 · 8 months · monthly snapshot~Sep 2021 – ~Nov 2022 · 14 months · monthly snapshot~Nov 2022 – ~Mar 2023 · 4 months · monthly snapshot~Mar 2023 – ~Apr 2024 · 13 months · monthly snapshot~Apr 2024 – ~Jul 2024 · 3 months · monthly snapshot~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshot~Sep 2024 – ~Apr 2025 · 7 months · monthly snapshot~Apr 2025 – ~Apr 2026 · 13 months · monthly snapshotApr 28, 2026 – present · 59 days · daily API

Change History

13 versions recorded
  1. Apr 28, 2026 — Present [daily]

    Recruiting

    Phase: NANone

  2. Apr 2025 — Apr 2026 [monthly]

    Recruiting NA

  3. Sep 2024 — Apr 2025 [monthly]

    Recruiting NA

  4. Jul 2024 — Sep 2024 [monthly]

    Recruiting NA

  5. Apr 2024 — Jul 2024 [monthly]

    Recruiting NA

Show 8 earlier versions
  1. Mar 2023 — Apr 2024 [monthly]

    Recruiting NA

  2. Nov 2022 — Mar 2023 [monthly]

    Recruiting NA

  3. Sep 2021 — Nov 2022 [monthly]

    Recruiting NA

  4. Jan 2021 — Sep 2021 [monthly]

    Recruiting NA

  5. Aug 2020 — Jan 2021 [monthly]

    Recruiting NA

  6. Feb 2019 — Aug 2020 [monthly]

    Recruiting NA

  7. Jun 2018 — Feb 2019 [monthly]

    Recruiting NA

  8. Jan 2017 — Jun 2018 [monthly]

    Recruiting NA

    First recorded

Jun 2013

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

This study aims to assess the differences in overall pain severity, pain management, and satisfaction during recovery period between two groups of children who either receive or do not receive additional education related to expectation and management of postoperative pain.

Contact Information

Sponsor contact:
  • Columbia University
Data source: ClinicalTrials.gov

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations