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Clinical observation for continuous intravenous infusion of lidocaine in painless colonoscopy

Clinical observation for continuous intravenous infusion of lidocaine in painless colonoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023746
Enrollment
Unknown
Registered
2019-06-10
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

colonoscopy

Interventions

Experimental Group:IV lidocaine
Control group:0.9% N.S

Sponsors

Affiliated Hospital of Xuzhou Medical University,
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 65 years; ASA grade between 1 to 3; colonoscopy time greater than 5 min., less than 1 hour.

Exclusion criteria

Exclusion criteria: Mental or mental illness, severe hypertension, NYHA cardiac function grade greater than grade II, bronchial asthma, sleep apnea syndrome, alcohol addiction, BMI = 30kg / m2, liver and kidney dysfunction, local anesthetic allergy, history of colectomy.

Design outcomes

Primary

MeasureTime frame
Numerical Rating Scale;—

Secondary

MeasureTime frame
Blood pressure;SPO2;amout of propofol;DSST;—

Countries

China

Contacts

Public ContactGuo Hui

Xuzhou Medical University

895531934@qq.com+86 15996933557

Outcome results

None listed

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