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Laryngeal Injuries After Anesthesia Induction With Sevoflurane and After Anesthesia Induction With Rocuronium

U

University of Rostock

Status

Completed

Conditions

Laryngeal Injuries

Treatments

Drug: Sevoflurane
Drug: Rocuronium

Study type

Interventional

Funder types

Other

Identifiers

NCT01591031
A 2011 124

Details and patient eligibility

About

Anesthesia induction with sevoflurane is not associated with an increased incidence or severity of laryngeal injuries compared with an anesthesia induction with a muscle relaxant.

Enrollment

60 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ear-nose-throat surgery
  • orotracheal intubation for surgery of the ear

Exclusion criteria

  • obesity
  • allergy against the study drugs
  • patients with a known or suspected difficult airway (Mallampati score 3 or 4 and a mouth opening < 3.5 cm).
  • all patients were examined by stroboscopy one day before surgery and were excluded from the study when preexisting pathologies of the vocal cords were found

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups

sevoflurane
Active Comparator group
Description:
anesthesia induction with propofol, remifentanil and sevoflurane
Treatment:
Drug: Sevoflurane
rocuronium
Active Comparator group
Description:
anesthesia induction with propofol, remifentanil and rocuronium
Treatment:
Drug: Rocuronium

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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