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Effect of Deksmedetomidine and Remifentanil in Extubation Agitation (EA)

D

Diskapi Yildirim Beyazit Training and Research Hospital

Status and phase

Unknown
Phase 4

Conditions

Agitation

Treatments

Drug: Saline
Drug: deksmedetomidine
Drug: Remifentanil

Study type

Interventional

Funder types

Other

Identifiers

NCT02104297
Agitation

Details and patient eligibility

About

To compare the effect of two different agents deksmedetomidine, remifentanil and placebo, agitation and recovery condition, on nasal septum operation.

Full description

Nasal septum operation cause agitation because of nasal package. This research aims determine which agent , deksmedetomidine remifentanil or placebo, is more beneficial to the patient.

Enrollment

90 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult patients

Exclusion criteria

  • patients with any sensitivity each drug

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups, including a placebo group

Deksmedetomidine infusion
Active Comparator group
Description:
To prevent agitation deksmedetomidine infused during operation and at the end of surgery agitation scor measured by Riker sedation agitation scale.
Treatment:
Drug: deksmedetomidine
Remifentanil infusion
Experimental group
Description:
To prevent agitation remifentanil infused during operation at the end of surgery agitation scor measured by Riker sedation agitation scale.
Treatment:
Drug: Remifentanil
Saline infusion
Placebo Comparator group
Description:
Saline infused during operation and at the end of surgery agitation scor measured by Riker sedation agitation scale.
Treatment:
Drug: Saline

Trial contacts and locations

1

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Central trial contact

Reyhan Polat, MD

Data sourced from clinicaltrials.gov

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