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Application of Virtual Reality (VR) combined with patient controlled intravenous analgesia in Postoperative Pain Management in Pediatric Patients

Application of Virtual Reality (VR) combined with patient controlled intravenous analgesia in Postoperative Pain Management in Pediatric Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119185
Enrollment
Unknown
Registered
2026-02-24
Start date
2024-06-21
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None

Interventions

A group:VR+Sufentanil 0.05ug/kg/h PCIA,establishing intravenous infusion access under VR+ standard treatment
B group:Sufentanil 0.05ug/kg/h PCIA, establishing intravenous infusion access under standard treatment

Sponsors

Plastic Surgery Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 10 Years

Inclusion criteria

Inclusion criteria: Children aged 5-10 who require postoperative analgesia for elective surgery.

Exclusion criteria

Exclusion criteria: 1. Epileptic seizure history, history of motion sickness; 2. cognitive dysfunction or inability to learn; 3. Sensory disorder; 4. Refused to sign the informed consent; 5. Claustrophobia.

Design outcomes

Primary

MeasureTime frame
Wong-Baker FACES Pain Rating Scale scores evaluated pre-intervention and immediately post-intervention at 1, 6, 12, and 24 hours after surgery;

Secondary

MeasureTime frame
Children’s mYPAS scores in the preoperative holding area;PCIA usage records;CPMAS scores assessed before and after the intervention in the post–operating room setting;Heart rate measured before and after the intervention after entering the operating room;Blood pressure measured before and after the intervention after entering the operating room;SpO2 assessed pre- and post-intervention following admission to the operating room";induction compliance ;FLACC scores assessed pre- and immediately post-intervention at 1, 6, 12, and 24 hours after surgery.;Wong-Baker FACES Pain Rating Scale score assessed during intravenous catheterization ;FLACC scale score assessed during intravenous catheterization;The types, timing and dosage of analgesic drugs used;Heart rate was measured pre- and immediately post-intervention at 1, 6, 12, and 24 hours after surgery;Blood pressure was measured pre- and immediately post-intervention at 1, 6, 12, and 24 hours after surgery;SpO2 was measured pre- and immediately post-intervention at 1, 6, 12, and 24 hours after surgery;

Countries

China

Contacts

Public ContactWei Lingxin

Plastic Surgery Hospital, Chinese Academy of Medical Sciences

weilx3934@sina.com+86 155 2200 2357

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026