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Two Different Preparations of Sevoflurane in Induction

I

Istanbul University

Status and phase

Completed
Phase 4

Conditions

Coughing on Induction
Vapors; Inhalation

Treatments

Drug: Sevoflurane

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

In our study we aim to study the effects of two preparations of Sevoflurane in vital capacity rapid inhalation induction.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing abdominal surgery

Exclusion criteria

  • Patients with any cardiovascular or respiratory disease, usage of any kind of sedative drug, expected airway difficulty and obese patients (BMI>35) will be excluded from the study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

200 participants in 2 patient groups

Sevoflurane A
Active Comparator group
Description:
Generic sevoflurane
Treatment:
Drug: Sevoflurane
Drug: Sevoflurane
Sevoflurane B
Active Comparator group
Description:
Orginal sevoflurane
Treatment:
Drug: Sevoflurane
Drug: Sevoflurane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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