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Remifentanil for Smooth Emergence in Elderly Patients

A

Ajou University School of Medicine

Status and phase

Completed
Phase 4

Conditions

Drug Usage

Treatments

Drug: Sevoflurane
Drug: Remifentanil

Study type

Interventional

Funder types

Other

Identifiers

NCT02334046
AJIRB-MED-CT4-14-383

Details and patient eligibility

About

Elderly patients show different pharmacokinetic and pharmacodynamic variables and usually need smaller doses of anaesthetic drugs than younger patients. The purpose of this study was to investigate the optimal effect-site concentration of remifentanil for preventing cough during emergence in elderly patients under sevoflurane and remifentanil anesthesia.

Enrollment

47 patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA physical status I or II undergoing endoscopic sinus surgery or septoplasty under balanced anesthesia with sevoflurane and remifentanil

Exclusion criteria

  • predicted difficult airway, body mass index > 30 kg/m2, history of obstructive sleep apnoea chronic respiratory disease or coughing, current smokers patients angiotensin converting enzyme-inhibitors

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

47 participants in 2 patient groups

Elderly
Experimental group
Description:
Remifentanil was maintained at predetermined effect-site concentration during the emergence period in elderly patients.
Treatment:
Drug: Sevoflurane
Drug: Remifentanil
Drug: Remifentanil
Adult
Active Comparator group
Description:
Remifentanil was maintained at predetermined effect-site concentration during the emergence period in adult patients.
Treatment:
Drug: Sevoflurane
Drug: Remifentanil
Drug: Remifentanil

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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