Effect of Dexmedetomidine in Preventing Cough and Postoperative Pain After Laryngeal Surgery for Cancer

Sponsor
Eye & ENT Hospital of Fudan University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03918889
Collaborator
(none)
120
1
2
19.1
6.3

Study Details

Study Description

Brief Summary

Background: During emergence from anesthesia for partial and total laryngectomy, severe airway reflex and systemic hypertension during recovery may lead to pneumoderm, hemorrhage, pneumomediastinum or pneumothorax. Dexmedetomidine is a selective α2-adrenoreceptor agonist that has sedative, analgesic, and sympatholytic properties. It has been reported dexmedetomidine can attenuate coughing reflex and prevent emergence agitation without delaying recovery and respiratory depression from general anesthesia. The purpose of this study was to investigate the effect of dexmedetomidine compared with midazolam on cough suppression and recovery quality during emergence from general anesthesia after partial and total laryngectomy.

Methods American Society of Anesthesiologists physical status I-II male adults undergoing elective laryngectomy under sevoflurane anesthesia were recruiting and randomly allocated to receive either dexmedetomidine(Group D, n = 60) infusion at 0.5 µg•kg-1 for 10 min before tracheotomy, then adjusted to 0.3µg•kg-1•h-1 or midazolam (Group M, n = 60) infusion at 0.05 mg•kg-1 ten minutes before tracheotomy, then adjusted to 0.02mg•kg-1•h-1. The primary outcome measure was the incidence and severity of cough. Hemodynamics, pain intensity [Visual Analogue Scale (VAS)] and Ramsay sedation scale (RSS) were also evaluated at awake, patients returning to ward from post anesthesia care unit (PACU),2h after surgery. postoperative sufentanil consumption, recovery time and the incidence of concerning adverse effects were recorded.

Condition or Disease Intervention/Treatment Phase
  • Drug: Dexmedetomidine Injectable Product
  • Drug: Midazolam injection
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
A Randomized Controlled Trial of the Effect of Dexmedetomidine Compared With Midazolam on Airway Reflex and Recovery Quality During Emergence From General Anesthesia After Partial and Total Laryngectomy
Actual Study Start Date :
May 1, 2019
Anticipated Primary Completion Date :
Dec 1, 2020
Anticipated Study Completion Date :
Dec 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: dexmedetomidine

patients receive dexmedetomidine infusion

Drug: Dexmedetomidine Injectable Product
dexmedetomidine infusion at 0.5 µg•kg-1 for 10 min before tracheotomy then adjusted to 0.3µg•kg-1•h-1

Experimental: midazolam

patients receive midazolam infusion

Drug: Midazolam injection
midazolam infusion at 0.05 mg•kg-1 ten minutes before tracheotomy then adjusted to 0.02mg•kg-1•h-1

Outcome Measures

Primary Outcome Measures

  1. The severity of cough [Time0:2hours after surgery]

    Coughing severity was classified using the 3-point scale.:1=mild (single) cough, 2=moderate (≤5 s) cough, and 3=severe (>5 s) cough.

Secondary Outcome Measures

  1. HR [Time0: 0 minute after arriving the operation room]

    Heart rate

  2. SBP [Time0: 0 minute after arriving the operation room]

    Systolic blood pressure

  3. DBP [Time0: 0 minute after arriving the operation room]

    Diastolic blood pressure

  4. SpO2 [Time0: 0 minute after arriving the operation room]

    Oxygen saturation using pulse oximetry

  5. HR [Time1:0 minute after drug administration]

    Heart rate

  6. SBP [Time1:0 minute after drug administration]

    Systolic blood pressure

  7. DBP [Time1:0 minute after drug administration]

    Diastolic blood pressure

  8. SpO2 [Time1:0 minute after drug administration]

    Oxygen saturation using pulse oximetry

  9. HR [Time2:0 minute after intubation]

    Heart rate

  10. DBP [Time2:0 minute after intubation]

    Diastolic blood pressure

  11. SBP [Time2:0 minute after intubation]

    Systolic blood pressure

  12. SpO2 [Time2:0 minute after intubation]

    Oxygen saturation using pulse oximetry

  13. HR [Time3:0 minute after medicine intervention]

    Heart rate

  14. DBP [Time3:0 minute after medicine intervention]

    Diastolic blood pressure

  15. SBP [Time3:0 minute after medicine intervention]

    Systolic blood pressure

  16. SpO2 [Time3:0 minute after medicine intervention]

    Oxygen saturation using pulse oximetry

  17. HR [Time4:0 minute after laryngectomy]

    Heart rate

  18. DBP [Time4:0 minute after laryngectomy]

    Diastolic blood pressure

  19. SBP [Time4:0 minute after laryngectomy]

    Systolic blood pressure

  20. SpO2 [Time4:0 minute after laryngectomy]

    Oxygen saturation using pulse oximetry

  21. HR [Time5:0 minute after the completion of surgery]

    Heart rate

  22. SBP [Time5:0 minute after the completion of surgery]

    Systolic blood pressure

  23. DBP [Time5:0 minute after the completion of surgery]

    Diastolic blood pressure

  24. SpO2 [Time5:0 minute after the completion of surgery]

    Oxygen saturation using pulse oximetry

  25. HR [Time6:0 minute after awareness]

    Heart rate

  26. SBP [Time6:0 minute after awareness]

    Systolic blood pressure

  27. DBP [Time6:0 minute after awareness]

    Diastolic blood pressure

  28. SpO2 [Time6:0 minute after awareness]

    Oxygen saturation using pulse oximetry

  29. HR [Time7:0 minute after departure from the PACU]

    Heart rate

  30. SBP [Time7:0 minute after departure from the PACU]

    Systolic blood pressure

  31. BDP [Time7:0 minute after departure from the PACU]

    Diastolic blood pressure

  32. SpO2 [Time7:0 minute after departure from the PACU]

    Oxygen saturation using pulse oximetry

  33. Pain intensity [Time0:2hours after surgery]

    Assessed by Visual Analogue Scale (VAS), (0, no pain; 10, the worst pain intolerable)

  34. Sedation [Time0: 2hours after surgery]

    Assessed by Ramsay sedation scale (RSS),1, Anxious or restless or both,2, Cooperative, orientated and tranquil,3,Responding to commands,4,Brisk response to stimulus,5,Sluggish response to stimulus,6, No response to stimulus.

  35. the incidence of adverse effects [Time0:2hours after surgery]

    desaturation,shivering,drowsiness, delirium,hypertension,hypotension,itching,arrhythmia,respiratory depression

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 65 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Subject scheduled for partial or total laryngectomy.

Exclusion Criteria:

Subject has respiratory disease; Subject has pharyngeal paraganglioma; Subject has cardiac disease; Uncontrolled hypertension; Subject has been taking β-adrenoreceptor blockers; Long-term abuse of alcohol (>6 months),opioids, or sedative-hypnotic drugs; Allergic to dexmedetomidine or midazolam; Subject has neuropsychiatric diseases; Operation time shorter than 1 h or longer than 4 h.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Anesthes iology, The Eye, Ear, Nose and Throat Hospital of Fudan University, Shanghai Medical College of Fudan University Shanghai Shanghai China 200031

Sponsors and Collaborators

  • Eye & ENT Hospital of Fudan University

Investigators

  • Study Director: Wenxian Li, PhD, Department of Anesthesiology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Eye & ENT Hospital of Fudan University
ClinicalTrials.gov Identifier:
NCT03918889
Other Study ID Numbers:
  • 2013005
First Posted:
Apr 18, 2019
Last Update Posted:
Jan 18, 2020
Last Verified:
Jan 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Eye & ENT Hospital of Fudan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 18, 2020