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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03311737
Other study ID # zs20170511
Secondary ID
Status Recruiting
Phase Phase 1
First received September 23, 2017
Last updated October 14, 2017
Start date September 19, 2017
Est. completion date March 31, 2018

Study information

Verified date September 2017
Source Shanghai Zhongshan Hospital
Contact yi li, Ph.D
Phone 13816836628
Email loulan_queen@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a single center, randomized, single blind study to compare the analgesic effect of different anesthesia and postoperative analgesic methods in uniportal VATS lung surgery.


Description:

Combining epidural with general anesthesia is regarded as the gold standard of general thoracic surgery. The uniportal VATS lung surgery have advantages of minimal invasive surgical incision, less postoperative pain, and so on. Whether general anesthesia can become an alternative method of combining epidural with general anesthesia in uniportal VATS lung surgery, investigators thus plan to make a comparison on intraoperative stress response, postoperative pain, immune function of patients,and hospital expenses.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date March 31, 2018
Est. primary completion date March 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Patients elective uniportal VATS lung surgery;

- BMI 18-30 kg/m2.

Exclusion Criteria:

- Patient refuse;

- ASA=3;

- Patients allergic to use anesthetics (propofol,rocuronium), patients with liver and/or kidney and/or mental dysfunction.

Study Design


Related Conditions & MeSH terms


Intervention

Combination Product:
general anesthesia
The investigators used general anesthesia preoperatively in uniportal VATS lung surgery
epidural anesthesia
The investigators used general anesthesia combined with epidural anesthesia preoperatively in uniportal VATS lung surgery

Locations

Country Name City State
China Zhongshan Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary visual analogue scale(VAS) This scale mainly reflects the patient's pain 1 year
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