Skip to content

Comparison of ultrasound-guided fascia iliaca compartment block, intravenous infusion low-dose dexmedetomidine, and low-dose dexmedetomidine combined with ultrasound-guided fascia iliaca compartment block in preventing emergence agitation of hip,outer thighs or knee-joint surgery in children

Comparison of ultrasound-guided fascia iliaca compartment block, intravenous infusion low-dose dexmedetomidine, and low-dose dexmedetomidine combined with ultrasound-guided fascia iliaca compartment block in preventing emergence agitation of hip, outer thighs or knee-joint surgery in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065680
Enrollment
Unknown
Registered
2022-11-11
Start date
2022-11-15
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

Emergence agitation

Interventions

Group F:Subjects receive ultrasound-guided fascia iliaca compartment block after general anesthesia intubation
Group D:Intravenous infusion Low-dose dexmedetomidine after general anesthesia intubation
Group FD:Subjects receive ultrasound-guided fascia iliaca compartment block combined with intravenous infusion Low-dose dexmedetomidine after general anesthesia intubation

Sponsors

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 2-12 years old,male or female; 2. Undergoing selective surgery which the surgical site included hip,outer thighs or knee-joint; 3. American Society of Anesthesiologists class I–II; 4. The guardian and child both signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Coagulation disorder; 2. Infection or tumour in the puncture site; 3. Sensory or motion dysfunction of lower limbs; 4. Severe cardiopulmonary complications; 5. Patients with cognitive dysfunction or mental disease; 6. Poor tolerance to surgery and anesthesia; 7. Patients with acute upper respiratory tract infection; 8. Patients who has recently taken painkillers(included opioid analgesics and non-steroids anti-inflammation drugs); 9. Allergy to anesthetics and study medications; 10. Lack of consent.

Design outcomes

Primary

MeasureTime frame
Incidence of agitation 30mins after emergence from anesthesia;

Secondary

MeasureTime frame
R-VAS;Time to remove endotracheal tube;Wake up time;

Countries

China

Contacts

Public ContactYuanyuan Hu

Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Huyuanyuan0608@163.com+86 15801771846

Outcome results

None listed

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