Acute and Chronic Pain After Video-assisted Thoracoscopic Surgery for Lung Cancer

Sponsor
Fudan University (Other)
Overall Status
Completed
CT.gov ID
NCT05478460
Collaborator
(none)
138
1
11.3
12.2

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate whether preoperative CT- guided hookwire localization would influence the incidence and intensity of acute and chronic pain after VATS.

Condition or Disease Intervention/Treatment Phase
  • Other: Hookwire localization

Detailed Description

Postoperative pain after thoracic surgery has gained recognition as a adverse outcome and head-scratching problem. The incidence of choric postoperative pain (CPSP) in thoracic surgery has been reported to be 20%-80%. However, there has been not an standard treatment for CPSP. Many study has showed the risk factors of CPSP in thoracic surgery, such as VATS type, operation time, duration of drainage, preoperative pain, repeat surgery, gender, postoperative chemotherapy or radiation therapy , etc. It is important that moderate-to-severe acute postoperative pain will be transformed into CPSP. That offers a new management goal in postoperative pain prevention.CT-guided hookwire localization have been proven to be benefical for VATS to diagnose and treat small pulmonary , it can shorten operation timing and increase surgery success rate. However, it causes roughly 23.8% severe pain and complaints included wire dislodgement, pneumothorax and haemorrhage during and after insertion. The question is whether or not the moderate-to-severe acute postoperative pain from hookwire localition will change the incidence and intensity of CPSP in VATS.

Nurses play a pivotal role in advanced practice, research, and education in the field of pain management. The pain management of hookwire localization may be a new vison in further research.

Study Design

Study Type:
Observational
Actual Enrollment :
138 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Acute and Chronic Pain After Video-assisted Thoracoscopic Surgery for Lung Cancer in Patients With Preoperative CT-guided Hookwire Localization
Actual Study Start Date :
Aug 10, 2021
Actual Primary Completion Date :
Jul 21, 2022
Actual Study Completion Date :
Jul 21, 2022

Arms and Interventions

Arm Intervention/Treatment
Group A

Before operation,patients were performed CT -guided hook wire localization(20G×120mm, PAJUNK medizintechnologie, Geisingen in Germany). patients were placed on a CT table in a suitable position(supine, prone, lateral) to obtain the shortest needle insertion route for their initial CT scan. Local anesthesia of the skin and planned puncture tract was performed using 10ml Lidocaine 1%. Next, the needle was inserted into or near the pulmonary nodule.

Other: Hookwire localization
Patients were performed CT -guided hook wire localization(20G×120mm, PAJUNK medizintechnologie, Geisingen in Germany). patients were placed on a CT table in a suitable position(supine, prone, lateral) to obtain the shortest needle insertion route for their initial CT scan. Local anesthesia of the skin and planned puncture tract was performed using 10ml Lidocaine 1%. Next, the needle was inserted into or near the pulmonary nodule.

Group B

without hookwire localization

Outcome Measures

Primary Outcome Measures

  1. postoperative incidence and intensity of chronic pain after surgery [at postoperative 3rd month]

    the incidence and severity(11-point numerical rating scale,0=painless, 10=woest pain)of pain was assessed after VATS operation

  2. postoperative incidence and intensity of chronic pain after surgery [at postoperative 6th month]

    the incidence and severity(11-point numerical rating scale, 0=painless, 10=worst pain)of pain was assessed after VATS operation

Secondary Outcome Measures

  1. postoperative length of stay in hospital [an average of 1 week]

    the days between postoperative 1st day and day of discharge from hospital

  2. satisfactory score [from the day discharge from hospital to postoperative 6th month]

    Likert score (from 1 to 5),higher scores mean a better outcome

  3. intensity of postoperative acute pain [from immediately after surgery(at postanesthesia care unit ) to postoperative 2nd day]

    the severity(11-point numerical rating scale, 0=no pain, 10=worst pain) after VATS operation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged 18-75

  • patients who underwent underwent CT-guided localization before VATS

  • ASA I-II

  • BMI 18.5-30

  • no serious complications after localization

  • sign informed consent

Exclusion Criteria:
  • could not complish underwent CT-guided localization

  • selfexpression or visual dysfunction

  • having emergency surgery

  • a severe psychiatric illness

  • having chronic pain problems in the chest area

  • Pregnant women

Contacts and Locations

Locations

Site City State Country Postal Code
1 270 Dongan Road, Fudan University Shanghai Cancer Center Shanghai China 200032

Sponsors and Collaborators

  • Fudan University

Investigators

  • Principal Investigator: Jun Zhang, PhD, Department of Anesthesiology, Fudan University Shanghai Cancer Center;

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jun Zhang, chairman of Department of Anesthesiology, Fudan University
ClinicalTrials.gov Identifier:
NCT05478460
Other Study ID Numbers:
  • pain assessment after VATS
First Posted:
Jul 28, 2022
Last Update Posted:
Aug 8, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jun Zhang, chairman of Department of Anesthesiology, Fudan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 8, 2022