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Effects of Dexmedetomidine on OI, RI and Inflammatory Factors in Patients Undergoing Palatopalatyngoplasty.

G

General Hospital of Ningxia Medical University

Status

Unknown

Conditions

Adverse Effect

Treatments

Drug: dexmedetomidine
Other: normal saline

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to investigate the efficacy of dexmedetomidine on oxygenation index, respiratory index and inflammatory factors, and to explore the protective effect of the dexmedetomidine on respiratory function in patients undergoing palatopalatyngoplasty.

Full description

Obstructive sleep apnea syndrome is common among people, especially among obese people, Which is characterized by periodic or complete upper airway obstruction and hypoxia during sleep. Intermittent hypoxia contributes to the lung damage by increased oxidative stress, inflammation. Some researchers suggested that dexmedetomidine can inhibit inflammatory reaction and lessen the damage of respiratory function. The aim of this study is to investigate the efficacy of dexmedetomidine on oxygenation index, respiratory index and inflammatory factors, and to explore the protective effect of the dexmedetomidine on respiratory function in patients undergoing palatopalatyngoplasty.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing palatopalatyngoplasty
  • ASA physical status II-III
  • Aged 18-65 years
  • BMI 18.5-30kg/m2

Exclusion criteria

  • Bradycardia
  • Atrioventricular block
  • Allergic to the drugs
  • Complicating pulmonary disease(including pulmonary infection,COPD, asthma and so on)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

80 participants in 2 patient groups, including a placebo group

Group D
Experimental group
Description:
40 patients receive a loading infusion of dexmedetomidine (1ug/kg)for 20min follow by a maintenance infusion (0.4ug/kg/h) continued until the end of the surgery
Treatment:
Drug: dexmedetomidine
Group C
Placebo Comparator group
Description:
40 patients receive matching placebo (normal saline)
Treatment:
Other: normal saline

Trial contacts and locations

1

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Central trial contact

Li Na; Ma Hanxiang

Data sourced from clinicaltrials.gov

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