Application of Comfort Treatment in Oral Outpatient Surgery: A randomized controlled trial

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900021516

Enrollment

Unknown

Registered

2019-02-25

Start date

2019-02-25

Completion date

Unknown

Last updated

2019-03-04

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

Conditions

Oral diseases

Interventions

group A:Midazolam

group D:Dexmedetomidine

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The patients were of AmericanSociety of Anesthesiology (ASA) physical status I or II, between 19 and 60 years old.

Exclusion criteria

Exclusion criteria: if they had a clinical history or electrocardiographic evidence of heart block, ischemic heart disease, asthma, sleep apnea syndrome, impaired liver or renal function, known psychiatric illness, diabetes, facial pain, psychological problems, smoking history, or chronicuse of sedative or analgesic drugs or opioids. Also excluded were those who refused to participate, were pregnant, or presented with preoperative inflammation at the site of surgery.

Design outcomes

Primary

Measure	Time frame
Ramsay;	—

Countries

China

Contacts

Public ContactWang Li

wli201608@163.com+86 027 87686055

Outcome results

None listed

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