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Endotracheal intubation with propofol and remifentanil alone for suspension laryngoscopic excision of vocal fold nodules: A patient-blinded, randomized, controlled study

Endotracheal intubation with propofol and remifentanil alone for suspension laryngoscopic excision of vocal fold nodules: A patient-blinded, randomized, controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002645
Enrollment
Unknown
Registered
2012-10-31
Start date
2010-07-01
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

vocal fold nodules

Interventions

1:Midazolam0.03mg/Kg+propofol3ug/ml +remifentanil4-6ug/ml+Cis-atracurium0.1mg/kg
2:Midazolam0.03mg/Kg+propofol3ug/ml +remifentanil4-6ug/ml

Sponsors

Department of Anesthesiology, the First Hospital of Jilin University, Changchun, China
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria were: age > 18 years and < 65 years, body mass index (BMI) of 18.5–25 kg/m2, class I or II physical status according to the American Society of Anesthesiologists (ASA) and Mallampati class (a measure predicting the ease of intubation) I or II, and scheduling for elective suspension laryngoscopic excision under IWMR.

Exclusion criteria

Exclusion criteria: The exclusion criteria were: a medical history of myopathy; a known history of allergy to propofol and/or remifentanil or drug abuse; and/or a previous history of upper respiratory tract infection within 3 weeks of enrollment, gastrointestinal reflux, intracranial pathology, suspected difficult airway, or serious cardiopulmonary or hepatorenal insufficiency.

Design outcomes

Primary

MeasureTime frame
post-anesthesia recovery times;

Countries

China

Contacts

Public ContactHaichun Ma
mahaichun2003@yahoo.com.cn+86 13578927386

Outcome results

None listed

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