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Effect of preoperative intravenous ibuprofen on postoperative analgesia in children

Effect of preoperative intravenous ibuprofen on postoperative analgesia in children

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101660
Enrollment
Unknown
Registered
2025-04-28
Start date
2023-10-11
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Hypospadias/tonsil hypertrophy

Interventions

Experimental group during tonsillectomy:intravenous ibuprofen
Control group in tonsillectomy:normal saline
Experimental group during urethroplasty:intravenous ibuprofen
Control group during urethroplasty:normal saline

Sponsors

Beijing Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 7 Years

Inclusion criteria

Inclusion criteria: 1) 2 to 7 years old; 2) Tonsillectomy/urethroplasty at selected time; 3) ASA I ~ II level; 4) Parents or legal guardians sign informed consent.

Exclusion criteria

Exclusion criteria: 1)Children undergoing emergency surgery; 2) Operation duration > 2 hours; 3) Postoperative hospitalization 10 times per hour);

Design outcomes

Primary

MeasureTime frame
The proportion of post-operative fentanyl supplementation;

Secondary

MeasureTime frame
The intraoperative dosage of remifentanil;The dosage of post-operative fentanyl supplementation;post-operative FLACC scores at each follow-up time point ;The post-operative NRS score of the children by the guardian;

Countries

China

Contacts

Public ContactJianmin Zhang

Beijing Children's Hospital

zhangjianmin@bch.com.cn+86 139 1029 9602

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026