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Application of propofol combined with intravenous lidocaine in pediatric colonoscopy: a randomized placebo-controlled study

Application of propofol combined with intravenous lidocaine in pediatric colonoscopy: a randomized placebo-controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000028927
Enrollment
Unknown
Registered
2020-01-08
Start date
2020-02-15
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

pediatric colonoscopy

Interventions

experimental group:Intravenous lidocaine
control group:Intravenous same volume of saline

Sponsors

Department of Anesthesiology, Guangdong Women and Children Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 10 Years

Inclusion criteria

Inclusion criteria: Aged 3-10 years, normal ECG examination.

Exclusion criteria

Exclusion criteria: With a history of congenital heart disease, liver insufficiency, major cardiac arrhythmia, and allergy to lidocaine.

Design outcomes

Primary

MeasureTime frame
The dosage of propofol;The dosage of sufentanil;—

Countries

China

Contacts

Public ContactYuan Chao

Guangdong Women and Children Hospital

fby329209549@126.com+86 18826122641

Outcome results

None listed

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