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Recruiting NCT04963751

NCT04963751 ERAS in Pediatric & Adolescent Gynecology Preoperative Counseling

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Clinical Trial Summary
NCT ID NCT04963751
Status Recruiting
Phase
Sponsor University of Colorado, Denver
Condition Enhanced Recovery After Surgery
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2022-09-08
Primary Completion 2027-01-31

Eligibility & Interventions

Sex Female only
Min Age 9 Years
Max Age 17 Years
Study Type INTERVENTIONAL
Interventions
Enhanced Recovery After Surgery (ERAS) Counseling to PatientsEnhanced Recovery After Surgery (ERAS) Counseling to Caregiver

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2022-09-08 with a primary completion date of 2027-01-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The Investigator propose a randomized trial that will assess whether participant involvement in pre-operative counseling for ERAS improves post-surgical pain scores. The Investigator will also assess participant compliance to ERAS-prescribed medications, and functionality (return to school). Each participant who is enrolled in the study will be assigned to 1) pre-operative counseling with participant's caregiver or 2) caregiver-only counseling.

Eligibility Criteria

Inclusion Criteria: * 9- 17 years of age * Patient is undergoing abdominal surgery and being managed under the ERAS protocol Exclusion Criteria: * Developmental delay (IQ \< 70) determined by documentation in medical record * Emergency or non-elective surgical cases * Patients who attend clinic appointments independently from their caregiver

Contact & Investigator

Central Contact

Patricia S Huguelet, MD

✉ patricia.huguelet@cuanschutz.edu

📞 (720)-777-2238

Principal Investigator

Patricia Huguelet, MD

PRINCIPAL INVESTIGATOR

University of Colorado, Denver

Frequently Asked Questions

Who can join the NCT04963751 clinical trial?

This trial is open to female participants only, aged 9 Years or older, up to 17 Years, studying Enhanced Recovery After Surgery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04963751 currently recruiting?

Yes, NCT04963751 is actively recruiting participants. Contact the research team at patricia.huguelet@cuanschutz.edu for enrollment information.

Where is the NCT04963751 trial being conducted?

This trial is being conducted at Aurora, United States.

Who is sponsoring the NCT04963751 clinical trial?

NCT04963751 is sponsored by University of Colorado, Denver. The principal investigator is Patricia Huguelet, MD at University of Colorado, Denver. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology