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Patient Satisfaction After Surgery for Otosclerosis Under Local ou General Anesthesia

NCT03888079 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 103

Last updated 2022-04-05

No results posted yet for this study

Summary

Main purpose of this study is to compare comfort level of patients, after otosclerosis surgery, under local or general anesthesia.

Conditions

  • Otosclerosis
  • Otosclerosis Surgery

Interventions

DRUG

Local anesthetic

1% or 2% lidocaine with 1:100,000 epinephrine, augmented by intravenous sedation and analgesia

DRUG

general anesthetic

Endotracheal intubation, intravenous narcotic agents, and inhaled agents

Sponsors & Collaborators

  • Rennes University Hospital

    lead OTHER

Principal Investigators

  • Benoit Godey, PH-PD · Rennes University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-11
Primary Completion
2021-03-03
Completion
2021-06-21

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03888079 on ClinicalTrials.gov