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Dexmedetomidine and Propofol in the Treatment of Emergence Agitation

Comparing the Efficacy of Dexmedetomidine and Propofol in the Treatment of Emergence Agitation Occurring in Adults After General Anesthesia: A Randomised Control Trial DP-TEA Trial

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04142840
Enrollment
120
Registered
2019-10-29
Start date
2019-11-01
Completion date
2021-08-30
Last updated
2020-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emergence Agitation

Brief summary

1. This clinical research aims to compare the effects of dexmedetomidine and propofol on the treatment of emergence agitation in adult patients after general anesthesia. 2. Half of participants will receive dexmedetomidine while the other half will receive propofol when emergence agitation happens.

Detailed description

As a common problem observed in pediatric patients after sevoflurane anesthesia, emergence agitations are investigated mainly in children.For adults,previous studies were almost about the efficacy of premedication on preventing emergence agitation. Once emergence agitation happens, there is still no guidelines established to recommend the medication usage in the post-anaesthesia care unit.So high-quality prospective clinical studies are required to provide evidence for emergence agitation treatment. Dexmedetomidine and propofol are both widely used in general anesthesia and can be acquired easily.When emergence agitation occurs,both injections are common choices in daily clinical administration on emergence agitation.To the investigator's knowledge ,propofol with a very quick onset is superior for anesthesia goals, but is without analgesia effects.While dexmedetomidine can produce sedation,analgesia,anxiolysis.So the investigators propose the hypothesis here that dexmedetomidine is prior to propofol on the treatment of emergence agitation in adults patients after general anesthesia.Therefore this research is undertaken to verify the hypothesis.

Interventions

DRUGDexmedetomidine

a selective α-2 adrenoceptor agonist which is widely used as an adjuvant to general anesthesia

DRUGPropofol

a short -acting medication that result in a decreased level of consciousness and lack of memory for events,widely used including the starting and maintenance of general anesthesia.

Sponsors

RenJi Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult patients aged 18-65 years old after general anesthesia * with informed consent provided.

Exclusion criteria

* age younger than 18 years or older than 65 years; * American Society of Anesthesiologists classification ≥Ⅲ; * preoperative lung dysfunction(including pneumonia,atelectasis,adult respiratory distress syndrome,acute lung injury and so on); * preoperative heart dysfunction(including sever cardiac coronary disease,unstable angina,LVEF≤30%,sick sinus syndrome,bradycardia:heart rate≤50bpm,second or third degree A-V block); * history of mental disease; * no informed consent provided; * uncontrolled hypertension(baseline blood pressure:SBP≥160mmHg or DBP≥110mmHg); * cancers; * enrolled in other researches within 90 days; * allergic to intervening medicine. * BMI less than 18 or more than 30 kg/m2.

Design outcomes

Primary

MeasureTime frameDescription
The recurrence rate of emergence agitation assessed by the Riker Sedation-Agitation Scale after the treatment of each group.1 day1. The Riker Sedation-Agitation Scale is raging from a maximum value of 7 to a minimum value of 1.Lower scores mean a better outcome. 2. A Riker Sedation-Agitation scale score of 5 or more than 5 will be considered as emergence agitation.

Secondary

MeasureTime frameDescription
Heart rate before and after intervention;1 dayHeart rate wil be recorded in beats per minute.
The consumption of sufentanil in the post-anaesthesia care unit;1 dayDuring the procedure,a dose of 0.01ug/kg sulfentanil will be given when numeric rating scale scores≥ 5 scores or the patient has a analgesia request; Numeric rating scale,with a maximum value of 10 and a minimum value of 0,is specifically as follows:0-3,slight pain;4-7,moderate pain;8-10,sever pain.Lower scores mean a better outcome.
Nausea and vomiting scores when leaving the post-anesthesia care unit.1 dayAccording the following scale with a maximum value of 3 and a minimum value of 0,is specifically as follows:0,no nausea;1,mild nausea;2,sever nausea requiring antiemetics;3,retching,vomiting or both.Lower scores mean a better outcome.
Riker Sedation-Agitation Scale scores before and after intervention;1 dayRiker Sedation-Agitation Scale is raging from a maximum value of 7 to a minimum value of 1.Lower scores mean a better outcome.
Recovering quality: recovery scale24 hours after surgery.The recovering quality is evaluated by the 40-item quality of recovery scale,with a maximum value of 200 and a minimum value of 0.Higher scores mean a better outcome.
Mean blood pressure before and after intervention;1 dayMean blood pressure will be recorded in millimeters of mercury.
Duration in the post-anaesthesia care unit1 dayThe total time from entering the post-anaesthesia care unit to leaving the post-anaesthesia care unit.

Countries

China

Contacts

Primary ContactSong Zhang, MD
zhangsong1031@163.com15150012530
Backup ContactWeifeng Yu, MD
yuweifeng@renji.com18918358260

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026