Study on the application of butorphanol in combination with dexmedetomodine on dressing changes of burned patients

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000032691

Enrollment

Unknown

Registered

2020-05-07

Start date

2020-06-01

Completion date

Unknown

Last updated

2020-05-18

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

Conditions

Burn injury

Interventions

experimental group:Dexmedetomidine combined with butorphanol

control group:saline combined with butorphanol

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Whose ages were between 20 and 60 years old, with total burn surface area (TBSA) from 10% to 30%, American Society of Anesthesiologists (ASA) physical status I or II.

Exclusion criteria

Exclusion criteria: Pregnant, allergic to opioids, had inhalation injuries, electrical injuries, mental problems and significant organ diseases.

Design outcomes

Primary

Measure	Time frame
VAS score;RSS score;MBP;HR;RR;SpO2;	—

Countries

China

Contacts

Public ContactXianchao Ding

The Affiliated Hospital of Jiangsu University

robertding3324@126.com+86 13862446335

Outcome results

None listed

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