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Randomized controlled clinical study of scalp nerve block in anesthesia and postoperative analgesia of craniosuture reconstruction

Randomized controlled clinical study of scalp nerve block in anesthesia and postoperative analgesia of craniosuture reconstruction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066131
Enrollment
Unknown
Registered
2022-11-25
Start date
2021-09-30
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Craniosynostosis

Interventions

Group A:General anesthesia+scalp nerve block

Sponsors

Children's Hospital of Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.5 Years to 2 Years

Inclusion criteria

Inclusion criteria: 1. Children who are selected for craniosuture reconstruction; 2. American Society of Anesthesiologists (ASA) Grade I~II; 3. Aged from 6 months to 2 years, male or female; 4. Children who are expected to have tracheal intubation removed within 2 hours after operation; 5. The guardian clearly understands and voluntarily participates in the study, and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. People with coagulation dysfunction; 2. The puncture point is infected; 3. Patients with serious heart, liver, kidney, brain and other important organ diseases; 4. Children who are participating in other clinical trials; 5. The guardian refuses to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
blood sugar;

Secondary

MeasureTime frame
mean arterial pressure;heart rate;FLACC;Press times of analgesic pump;

Countries

China

Contacts

Public ContactZou Tianxiao

Children's Hospital of Shanghai

zouu163@163.com+86 186 6322 9539

Outcome results

None listed

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