The influences of pre-filled syringe and PVC Infusion tube to propofol injection pain

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-12003170

Enrollment

Unknown

Registered

2012-12-22

Start date

2013-04-29

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

The injection pain of propofol

Interventions

Ampoul group:Intravenous inject propofol packaged with glass ampoul

Pre-filled syringe group:Intravenous inject propofol packaged with pre-filled syringe

Ampoul + PVC tube group:Intravenous inject propofol packaged with glass ampoul through PVC tube

Pre-filled syringe + PVC tube group:Intravenous inject propofol packaged with pre-filled syringe through PVC tube

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 65; 2. ASA I-III; 3. People accepted the informed consent file.

Exclusion criteria

Exclusion criteria: 1. participated in other clinical trials four weeks ago the start of this study; 2. Taking neurological drugs 2 weeks ago the beginning of the experiment; 3. Respiratory depression, (lung) airway obstruction or hypoxia; 4. Cardiac disorders (level II and above level II cardiac function); 5. Liver, kidney dysplasia (indicators higher than the normal twice); 6. Brain disease, abnormal judgment ability; 7. allergy to Propofol; 8. Drugs and/or alcohol abuse; 9. Pregnant or lactating women.

Design outcomes

Primary

Measure	Time frame
pain level;	—

Secondary

Measure	Time frame
blood pressure;heart rate;blood oxygen saturation;	—

Countries

China

Contacts

Public ContactQI Wu

wuqimed@126.com+86 18660150557

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 8, 2026