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Effect of intravenous dexmedetomidine infusion on postoperative pulmonary complications in elderly laparoscopic patients

Effect of intravenous dexmedetomidine infusion on postoperative pulmonary complications in elderly laparoscopic patients

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075746
Enrollment
Unknown
Registered
2023-09-14
Start date
2023-09-15
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Postoperative Pulmonary Complications

Interventions

Dexmedetomidine Group(DEX):Intravenous dexmedetomidine infusion
Control Group(C):Intravenous physiological saline infusion

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1: The patient is older than or equal to 65 years old 2: Proposed laparoscopic gastrointestinal surgery 3: American Society of Anesthesiologists physical status ?~?

Exclusion criteria

Exclusion criteria: 1: Dexmedetomidine allergy or contraindication 2: Suffer from other serious systemic disease (serious heart, kidney, or liver and lung disease) 3: Drug and alcohol addiction and mental disorders 4: BMI>30kg/m² 5: Expected to be transferred to ICU after surgery 6: The operation is expected to less than two hours 7: A history of upper respiratory or lung infection in the past 4 weeks 8: There was severe pleural effusion and atelectasis before surgery

Design outcomes

Primary

MeasureTime frame
Score of Postoperative Pulmonary Complications;

Secondary

MeasureTime frame
Pulmonary Surfactant Related Protein-D (SP-D);IL-6;TNF-a;Blood Gas Analysis;

Countries

China

Contacts

Public ContactSun Defeng

The First Affiliated Hospital of Dalian Medical University

sdf-yl@163.com+86 180 9887 6191

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 16, 2026