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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03612440
Other study ID # MHX07
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date April 30, 2019

Study information

Verified date August 2018
Source General Hospital of Ningxia Medical University
Contact Ma Hanxiang
Phone +86-13519591508
Email mahanxiang@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 80
Est. completion date April 30, 2019
Est. primary completion date April 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
dexmedetomidine
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
Other:
normal saline
receive matching placebo (equal volum of normal saline)

Locations

Country Name City State
China General Hospital of Ningxia Medical University Yinchuan Ningxia

Sponsors (1)

Lead Sponsor Collaborator
General Hospital of Ningxia Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Oxygenation Index Arterial blood samples were sampled before anaesthesia induction and immediately after surgery for the oxygenation index by using blood gas analyzer. Intraoperative and immediately after surgery
Primary The Respiratory Index Arterial blood samples were sampled before anaesthesia induction and immediately after surgery for the respiratory index by using blood gas analyzer. Intraoperative and immediately after surgery
Secondary Change of tumor necrosis factor-a before anesthesia and immediately after surgery Blood samples were sampled before anaesthesia induction and immediately after surgery for the serum tumor necrosis factor-a,which were analyzed by using enzyme linked immunosorbent assay (ELISA). Intraoperative and immediately after surgery
Secondary Change of interleukin-6 before anesthesia and immediately after surgery Blood samples were sampled before anaesthesia induction and immediately after surgery for the serum interleukin-6, which were analyzed by using enzyme linked immunosorbent assay (ELISA). Intraoperative and immediately after surgery
Secondary Change of interleukin-10 before anesthesia and immediately after surgery Blood samples were sampled before anaesthesia induction and immediately after surgery for the serum interleukin-10, which were analyzed by using enzyme linked immunosorbent assay (ELISA). Intraoperative and immediately after surgery
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