Outcomes of Pediatric Robotic Surgery at a Tertiary Children's Hospital

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-18
SponsorMeyer Children's Hospital IRCCS

About this trial

This is a single-center retrospective observational cohort study evaluating surgical and clinical outcomes in pediatric patients undergoing robotic surgery at a tertiary children's hospital.

All consecutive patients younger than 18 years who underwent robotic-assisted procedures (digestive, urologic, gynecologic, or thoracic surgery) between January 2025 and December 2025 at Meyer Children's Hospital IRCCS will be included.

The primary objective is to describe postoperative complications within 30 days. Secondary objectives include conversion to open surgery, reintervention and readmission rates, length of hospital stay, postoperative pain, recovery parameters, and recurrence of the underlying disease within 12 months.

Data will be collected retrospectively from electronic medical records, operative registries, laboratory reports, and follow-up documentation up to 12 months after surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age < 18 years at the time of surgery

Underwent robotic-assisted surgical procedure (digestive, urologic, gynecologic, or thoracic surgery)

Surgery performed between January 2025 and December 2025 at Meyer Children's Hospital IRCCS

Availability of essential clinical and perioperative data in the medical record

Disqualifiers

Missing essential clinical or postoperative data required for analysis

Documented opposition to the use of clinical data for research purposes

Trial population

Pediatric patients undergoing robotic-assisted surgery at Meyer Children's Hospital IRCCS between January 2025 and December 2025.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 1 trial group
Group A: Pediatric Robotic Surgery Cohort

Trial outcomes

Primary outcomes

1

Postoperative Complications Within 30 Days

Occurrence of postoperative complications within 30 days after robotic-assisted surgery, classified according to the Clavien-Dindo grading system when applicable and documented in the medical record.

Time frame
30 days after surgery

Secondary outcomes

1

Reintervention Rate

Unplanned surgical reintervention within 30 days after the index robotic-assisted procedure.

Time frame
30 days after surgery
2

Hospital Readmission Rate

Unplanned hospital readmission occurring within 30 days after discharge from the index hospitalization.

Time frame
30 days after discharge
3

Postoperative Pain (VAS Score)

Pain intensity measured using the Visual Analog Scale (VAS) every 6 hours during the first 72 postoperative hours, as recorded in routine clinical documentation.

Time frame
72 hours after surgery
4

Time to Resumption of Oral Feeding

Time from surgery to resumption of oral feeding as documented in the medical record.

Time frame
Within 48 hours after surgery

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: