Clinical research of the analgesic effects of the dezocine and dexmedetomidine to the burnt patients during dressing change

Status

Recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-OPh-16008968

Enrollment

Unknown

Registered

2016-08-04

Start date

2016-08-01

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

burn

Interventions

A:dezocine and dexmedetomidine

B:dezocine

Eligibility

Sex/Gender

All

Age

16 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18-60 years; Burn area >5%TBSA.

Exclusion criteria

Exclusion criteria: HR < 70/min; Bp < 90/60 mmHg; Allergic to opioid drugs; Craniocerebral diseases; Arrhythmia; Chronic respiratory disease, chronic hypoxia.

Design outcomes

Primary

Measure	Time frame
VAS;	—

Countries

China

Contacts

Public ContactXue Wenjun

Shandong provincial hospital

xuewenjun708@sina.com+86 15168887991

Outcome results

None listed

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