The clinical research of program plan sedative for non-mechanically ventilated critically ill patients prescribing Dexmedetomidine

The clinical research of program plan sedative for non-mechanically ventilated critically ill patien

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-14004880

Enrollment

Unknown

Registered

2014-06-30

Start date

2014-08-01

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

postoperative patients

Interventions

A:nfuse sedative according to the program plan sedat

B:infuse sedative according to the status of patient

Eligibility

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Older than 18 years;2.The patients who would be transferred to ICU after surgery.

Exclusion criteria

Exclusion criteria: 1.Delirious patients; 2.Heart rate less than 70 bpm; 3.Ill associated with neurological-muscular joints,such as myasthenia gravis; 4.Fi02 less than 200; 5.Taking sedatives or opioid medicines regularly over a long period of time; 6.Patients with pregnancy.

Design outcomes

Primary

Measure	Time frame
Delirium;unpleasant experience;CRP;	—

Countries

China

Contacts

Public ContactMin Peng

tjpengmin@126.com+86 13602177443

Outcome results

None listed

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