Dexmedetomidine improves intubating conditions in children after induction with propofol and remifentanil without muscle relaxants

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TQR-14004833

Enrollment

Unknown

Registered

2014-06-17

Start date

2013-06-10

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

Clinical pharmacology

Interventions

D:induced by the infusion of dexmedetomidine 1 ug/kg

Control:0.9% NS

Eligibility

Sex/Gender

All

Age

5 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Aged 5 to 10 years old; 2. ASA I; 3. Underwent elective surgery plastic surgery; 4. Guardian agree to the scheme and sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Upper respiratory tract infection within three weeks; 2. Difficult airway history; 3. Obesity.

Design outcomes

Primary

Measure	Time frame
ease of performing the laryngoscopy;vocal cord condition;coughing;limb movement;jaw relaxation;mean arterial pressure;heart rate;	—

Contacts

Public ContactDengxiao Ming

Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

dengxiaoming2003@sina.com+86 010 88772082

Outcome results

None listed

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