Skip to content

Dreaming during sevoflurane or propofol short-term sedation: a randomized controlled trial

Dreaming during sevoflurane or propofol short-term sedation: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12001938
Enrollment
Unknown
Registered
2012-02-13
Start date
2009-05-15
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

Dream

Interventions

Propofol group:propofol (1.5 - 2.5 mg/kg) and one bolus of 1ug/kg of fentanyl intravenously
Sevoflurane group:8% sevoflurane and one bolus of 1ug/kg of fentany

Sponsors

the First Affiliated Hospital, Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 46 Years

Inclusion criteria

Inclusion criteria: 1. to be aged 20-46 yrs; 2. to be ASA I; 3. to be undergoing first-trimester surgical abortion; 4. to be less than 10 weeks gestational age; 5. had oral bowel preparation.

Exclusion criteria

Exclusion criteria: 1. had an inadequate comprehension of the Chinese language; 2. were diagnosed with a psychotic disorder.

Design outcomes

Primary

MeasureTime frame
The modified Brice questionnaire;a five-point Likert scale;the Hospital Anxiety and Depression Scale;educational level;home dreaming recall frequency;BIS values;an Observer’s Assessment of Alertness/Sedation (OA);sedation time;the time to eye opening;the time to interview;

Countries

China

Contacts

Public ContactKai Wang
aywangkai@126.com+86 13805512494

Outcome results

None listed

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