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Clinical study of small-dose esketamine pretreatment for prevention of propofol-induced injection pain in children

Clinical study of small-dose esketamine pretreatment for prevention of propofol-induced injection pain in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096697
Enrollment
Unknown
Registered
2025-02-05
Start date
2025-02-10
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

Propofol-induced injection pain

Interventions

Esketamine group:Esketamine injection was intravenously injected, and 45 seconds later, propofol was intravenously injected.
Lidocaine group:Mixture of propofol and lidocaine was injected intravenously 45 seconds after the same volume of normal saline was injected intravenously.

Sponsors

Anhui Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1.Children undergoing elective short operation (< one hour), aged 2-10 years; 2.ASA grade ? or ?; 3.Guardians agree to sign the informed consent form

Exclusion criteria

Exclusion criteria: 1. Allergy to anesthetic drugs; 2. Combined with cardiovascular, hepatic, renal or psychiatric diseases, history of seizures or intracranial hypertension; 3. The history of upper respiratory tract infection within the last 1 weeks; 4. Obesity (BMI>=95% for age and sex); 5. Crying when you enter the house.

Design outcomes

Primary

MeasureTime frame
Propofol injection pain;

Secondary

MeasureTime frame
Hemodynamics;Emergence agitation score, PAED;Adverse reactions;

Countries

China

Contacts

Public ContactLi Chen

Anhui Children's Hospital

chlmm2009@sina.com+86 153 0569 3511

Outcome results

None listed

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