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Dexmedetomidine to Improve Outcomes During Emergence From Retroperitoneal Laparoscopic Surgery (DEALS)

A

Air Force Military Medical University of People's Liberation Army

Status

Completed

Conditions

Anesthesia

Treatments

Other: loading dose
Other: sustaining dose
Drug: dexmedetomidine

Study type

Interventional

Funder types

Other

Identifiers

NCT02316236
XJH-A-2014-6-22-01

Details and patient eligibility

About

The study is to observe whether dexmedetomidine could reduce agitation during emergence from general anesthesia in patients undergoing retroperitoneal laparoscopic surgery.

Full description

Agitation during emergence is frequent after retroperitoneal urologic surgery. Dexmedetomidine is alpha-2 receptor agonist which shows sedative and algesic effect. In this study we will compare the effect of dexmedetomidine given by different protocols on emergence agitation.

Enrollment

66 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients scheduled for retroperitoneal laparoscopic surgery
  • Patients with written informed consent

Exclusion criteria

  • Patients with difficulty of communication
  • Patients with risk of obstructive sleeping apnea syndrome

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

66 participants in 2 patient groups

dexmedetomidine loading dose
Experimental group
Description:
dexmedetomidine is given at load dose
Treatment:
Drug: dexmedetomidine
Other: loading dose
dexmedetomidine sustaining dose
Experimental group
Description:
dexmedetomidine is given at sustaining dose
Treatment:
Drug: dexmedetomidine
Other: sustaining dose

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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