Skip to content

Compare the Analgesic Effect of Different Anesthesia and Postoperative Analgesic Methods in Uniportal VATS Lung Surgery

Compare the Analgesic Effect of Different Anesthesia and Postoperative Analgesic Methods in Uniportal VATS Lung Surgery

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03311737
Acronym
CDAAMIUVLS
Enrollment
100
Registered
2017-10-17
Start date
2017-09-19
Completion date
2018-03-31
Last updated
2017-10-17

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

Conditions

Postoperative Pain, Single-incision Thoracoscopic Surgery

Brief 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.

Detailed 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.

Interventions

COMBINATION_PRODUCTgeneral anesthesia

The investigators used general anesthesia preoperatively in uniportal VATS lung surgery

COMBINATION_PRODUCTepidural anesthesia

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

Sponsors

Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
visual analogue scale(VAS)1 yearThis scale mainly reflects the patient's pain

Countries

China

Contacts

Primary Contactyi li, Ph.D
loulan_queen@163.com13816836628
Backup Contactxiangting li, B.S.
524646417@qq.com13671864990

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026