FindTrial
Sign In

Dexmedetomidine-Fentanyl versus Propofol–Fentanyl for patients of flexible bronchoscopy: a randomized study

Dexmedetomidine-Fentanyl versus Propofol–Fentanyl for patients of flexible bronchoscopy: a randomized study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003904
Enrollment
Unknown
Registered
2013-11-27
Start date
2013-12-01
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

Dexmedetomidine-Fentanyl versus Propofol–Fentanyl for patients of flexible bronchoscopy

Interventions

DF:dexmedetomidine-fentanyl
PF:propofol–fentanyl

Sponsors

Department of Anesthesiology, The Second Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: The patients, aged between 20–75 years, with American Society of Anesthesiologists (ASA) physical classification system status of I–III.

Exclusion criteria

Exclusion criteria: psychological disorders; hypersensitivity or allergy to the study drugs; uncontrolled hypertension (uncontrolled hypertension with blood pressure higher than 140/90 mmHg); major abnormalities of liver function; ischemic heart disease and severe respiratory disease.

Design outcomes

Primary

MeasureTime frame
Pulse oxygen saturation;Heart rate;systolic blood pressure;diastolic blood pressure;cough scores;discomfort scores;recovery times;times of additional lidocaine;modified observer’s assessment of alert /sedation;adverse event;—

Countries

China

Contacts

Public ContactTieli Dong

The Second Affiliated Hospital of Zhengzhou University

tlddtl@126.com+86 13783692658

Outcome results

None listed

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