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Study of standard protocol of postoperative analgesia after pediatric neurosurgery

Study of standard protocol of postoperative analgesia after pediatric neurosurgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOC-15007676
Enrollment
Unknown
Registered
2015-12-20
Start date
2016-02-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Pediatric neurosurgery postoperative pain

Interventions

1 to 6 years Control group:saline
1 to 6 years Fentanyl group:Fentanyl
1 to 6 years Morphine group:Morphine
1-to 6 years Tramadol group:Tramadol
7 to 12 years Control group:saline
7 to 12 years Fentanyl group:Fentanyl
7 to 12 years Morphine group:Morphine
7-to 12 years Tramadol group:Tramadol

Sponsors

Beijing Tiantan Hospital affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Aged 1-12 years old; 2. ASA grade 1 to grade 3; 3. the children of Intracranial tumor resection.

Exclusion criteria

Exclusion criteria: 1) psychological disorders; 2) Airway abnormalities, High reaction airway disease; 3) cant pull out endotracheal intubation after surgery; 4) hematoma after surgery 3 days or second operation of children with serious cerebral edema.

Design outcomes

Primary

MeasureTime frame
FLACC scores;Numeric Rating Scale;Wong - Baker facial expression score;doses of analgesia;press numbers of analgesia pump;

Secondary

MeasureTime frame
patients‘ status during operation;operative complications;

Countries

China

Contacts

Public ContactLi-xin An
anlixin8120@163.com+86 13810248120

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 3, 2026