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The application of scalp block combined with general anesthesia in children undergoing craniotomy

The application of scalp block combined with general anesthesia in children undergoing craniotomy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001707
Enrollment
Unknown
Registered
2011-11-11
Start date
2011-12-01
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

clinical anesthesia

Interventions

A:Saline scalp block combined with general anesthesia
B:0.25% ropivacaine scalp block combined general anesthesia

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
No minimum to 14 Years

Inclusion criteria

Inclusion criteria: (1) ASA 1-2; (2) Aged 0 to 14 years old; (3) Selective craniotomy, consciouness before surgery; (4) The skin incision can be blocked by scalp block; (5) No cardiac,pulmonary, hepatic or kidney disease; (6) No vasoactive drugs preoperatively; (7) Parents are well educated (high school and above).

Exclusion criteria

Exclusion criteria: (1) History of neurosurgery; (2) Pain from places other than head; (3) Possible unconsciouness due to craniotomy; (4) With skull fracture or defect close to the inject spots; (5) Hypertension preoperatively; (6) Unable to perform FLACC or VAS assessment; (7) Allergies to any drugs that are to be administered during the study; (8) Taken analgesics more than 2 weeks preoperatively.

Design outcomes

Primary

MeasureTime frame
dosage of opioids during surgery;nausea;vomiting;local anesthetics toxicity;hematoma;Bradycardia;

Secondary

MeasureTime frame
dosage of general anesthetics during surgery;extubation time;awake time;heart rate during surgery;blood pressure during surgery;postoperative FLACC score;postoperative VAS score;dosage of analgesics postoperativel;

Countries

China

Contacts

Public ContactWu Chaoran
wuchaoran@yahoo.com+86 18980601146

Outcome results

None listed

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