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Propofol requirement for Induction of unconsciousness in patients with hearing disorder: A prospective cohort study

Propofol requirement for Induction of unconsciousness in patients with hearing disorder: A prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-16008741
Enrollment
Unknown
Registered
2016-06-29
Start date
2016-06-01
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

hearing disorder

Interventions

Two groups:target controlled infusion of propofol

Sponsors

First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) physical status I and I I patients aged 16 to 66 years and body weight from 30 to 90?kg and body mass index (BMI) 18–30 kg/m2 who were undergoing general anesthesia for different elective surgeries were included in our study.

Exclusion criteria

Exclusion criteria: 1. allergy to the agents used in the study; 2. difficult airway; 3. receiving anesthetic premedicationhepatic; 4. renal impairment; 5. uncontrolled hypertension; 6. coronary artery disease; 7. diabetes.

Design outcomes

Primary

MeasureTime frame
BIS;—

Secondary

MeasureTime frame
eyelash reflex;—

Countries

China

Contacts

Public ContactQinjun Chu

First Affiliated Hospital of Zhengzhou University

jimmynetchu@163.com+86 13643711142

Outcome results

None listed

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