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Effect of dexmedetomidine combined with escloramine on analgesia and postoperative depression in patients with severe burn injuries

Effect of dexmedetomidine combined with escloramine on analgesia and postoperative depression in patients with severe burn injuries

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061052
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

Burn

Interventions

Es group:Small doses of esketamine are given intravenously
Control group:Intravenous injection of an equal volume of 0.9% normal saline

Sponsors

The Affiliated Hospital of Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adults under the age of 60 years old; 2. ASA Grade II to III; 3. Burn area 30%-60%, burn depth of deep II degree and III degree; 4. The burn site involves the trunk and limbs of the body, and there is no serious liver and kidney function damage; 5. Primary school and above education level, able to do questionnaire surveys.

Exclusion criteria

Exclusion criteria: 1. Patients with serious primary diseases such as cardiovascular, cerebrovascular, hepatic and renal and hematopoietic systems; 2. Patients with severe burn fluid exudation period, wound repair period and rehabilitation period, patients with serious complications; 3. Patients with mental disorders and difficulty communicating; 4. History of drug allergies, severe liver and kidney dysfunction, blood system dysfunction and severe system symptoms such as sepsis, high fever and chills; 5. Tracheostomy has been performed with burns from special parts such as the respiratory tract; 6. Patients or patients' families are reluctant to participate in the study.

Design outcomes

Primary

MeasureTime frame
sas;

Secondary

MeasureTime frame
Comparison of hemodynamic indicators at different time points;Comparison of intraoperative cardiovascular adverse events;Postoperative pain level;

Countries

China

Contacts

Public ContactZhang Zhongjun

The Affiliated

zzj315@vip.sina.com+86 13961802567

Outcome results

None listed

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