Study on the Sedative Mode of Retention of Tracheal Intubation in intensive care unit

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1800016017

Enrollment

Unknown

Registered

2018-05-07

Start date

2018-06-01

Completion date

Unknown

Last updated

2018-05-14

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

Conditions

oral cancer

Interventions

Group A:midazolam

Group B:dexmedetomidine

Group C:propofol

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The patients who indwelled nasal tracheal duct in ICU after oral repair by forearm flap needed sedative treatment were enrolled in this study. They were aged from 18 years or older with American Society of Anesthesiologists (ASA) physical status I or II undergoing selective operation. Radical surgeries included primary enlargement resection, cervical lymphadenectomy, repair of oral and maxillofacial tissue defects by forearm flap and small vascular anastomosis.

Exclusion criteria

Exclusion criteria: 1. had severe chronic liver disease; 2. had acute myocardial infarction or severe heart failure; 3. had drug dependence or alcoholism or a psychological illness or severe cognitive dysfunction; 4. pregnant and lactating; or 5. were allergic to midazolam, propofol and dexmedetomidine.

Design outcomes

Primary

Measure	Time frame
CRP;	—

Countries

China

Contacts

Public ContactWang Li

Stomatology Hospital, Wuhan University

198jimmy@163.com18571715252

Outcome results

None listed

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