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A cross-over study to evaluate a new parameter PI for objective assessment of pain

A cross-over study to evaluate a new parameter PI for objective assessment of pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IDR-16008884
Enrollment
Unknown
Registered
2016-07-22
Start date
2016-07-30
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

pain

Interventions

A:lidocaine cream first
B:VE cream first

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 59 years old; BMI 18 to 25 kg/m2; 2. healthy volunteers: vital signs normal (axillary temperature 36.1 ~ 37 ?, HR 60 ~ 100 bpm, RR, 12 ~ 24 times/min, 90 MMHG 0.8; Normal exercise capacity(able to climb four flights of stairs); 3. the right forearm without sensory disturbance, without scar; 4. voluntarily accept the test and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. VE local and/or anaesthetic cream allergies; 2. female volunteers menstruating/pregnancy/lactation; 3. history of liver disease, kidney disease; 4. SAS indicates anxiety status; 5. with mental disease or nervous system diseases.

Design outcomes

Primary

MeasureTime frame
PI;

Countries

China

Contacts

Public ContactYi Feng

Peking University People's Hospital

yifeng65@sina.com+86 010-88325590

Outcome results

None listed

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