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Effects of dexmedetomidine on perioperative stress response in combined general anesthesia

Effects of dexmedetomidine on perioperative stress response in combined general anesthesia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17012237
Enrollment
Unknown
Registered
2017-08-03
Start date
2017-08-09
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

General anesthesia of laparoscopic surgery

Interventions

Group D:Intravenous infusion of dexmedetomidine before induction of anesthesia
Group C:Intravenous infusion of same volume normal saline before induction of anesthesia

Sponsors

Department of Anesthesiology, Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 68 Years

Inclusion criteria

Inclusion criteria: Forty patients with American Society of Anesthesiologists (ASA) I or II, scheduled for elective laparoscopic surgery under general anesthesia,all genders, aged 18-68 years,body mass index less than 30 kg/m2, with normal hepatic or renal function, without uncontrolled hypertension and/or diabetes mellitus, severe heart and lung diseases, and signed informed consent form before anesthesia, will be prospectively studied.

Exclusion criteria

Exclusion criteria: Patients with a history of allergy to dexmedetomidine, severe cardiac conduction block, evidence of pregnancy, a (family) history of malignant hyperthermia, having drug and alcohol dependency, refused to sign an informed consent form, or total time of target-controlled infusion of sufentanil is more than 4 hours, will be excluded.

Design outcomes

Primary

MeasureTime frame
Blood cortisol concentration;Hemodynamic changes;Blood glucose concentration;

Secondary

MeasureTime frame
Blood C-reactive protein concentration;blood gas analysis;Recovery profile;Adverse effect;

Countries

China

Contacts

Public ContactYan Zhao

Department of Anesthesiology, Peking University Third Hospital

zhaoyan2004@263.net+86 13911666385

Outcome results

None listed

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