- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05187390
Incidence of Chronic Pain After Video-Assisted Thoracic Surgery
Video-assisted thoracic surgery (VATS) is frequently performed in thoracic surgery. It is widely accepted that VATS causes acute pain. Many factors such as postoperative analgesia treatment plan, operation time, number of chest tubes, and duration of chest tube stay can affect acute pain. This acute pain prolongs the discharge time of the patients and increases the frequency of postoperative pulmonary complications and postoperative morbidity. Postoperative acute pain may cause chronic pain in the later period, and may adversely affect the quality of life of the patients.
This study, it was aimed to analyze the symptoms of chronic pain in the 1st and 3rd months postoperatively in patients who had undergone VATS.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Oya Kaybal, MD
- Phone Number: 00905438760088
- Email: kaybaloya@gmail.com
Study Contact Backup
- Name: Musa Zengin, MD
- Phone Number: 00905307716235
- Email: musazengin@gmail.com
Study Locations
-
-
Ankara
-
Keçiören, Ankara, Turkey, 06290
- Recruiting
- Ankara Atatürk Chest Disease and Chest Surgery Training and Research Hospital
-
Contact:
- Oya Kaybal, MD
- Phone Number: +905079193765
- Email: kaybaloya@gmail.com
-
Contact:
- Musa Zengin, MD
- Phone Number: +905307716235
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Patients between the ages of 18-65 years, in the ASA I-II-III risk group, with a BMI between 18-35 kg/m2 and undergoing VATS will be included in our study.
Patients under the age of 18 years and over the age of 65 years, with an ASA score of IV and above, with a BMI below 18 kg/m2 and above 35 kg/m2, who were operated under emergency conditions, and who received chronic pain treatment will be excluded from the study.
Description
Inclusion Criteria:
- Age between 18 and 65 years
- American Society of Anesthesiologists physical status I-II-III
- Body mass index between 18-35 kg/m2
- Patients undergoing elective VATS
Exclusion Criteria:
- Advanced cancer
- History of chronic analgesic therapy
- Patients with previous thoracic surgery
- Patients who were operated under emergency conditions
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain scores at 1st months.
Time Frame: Chronic pain symptoms at 1st months
|
Chronic pain symptoms will be assessed using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain).
Neuropathic pain symptoms (Burning, stabbing, electric shock-like pain, tingling, numbness, pins, and needles feeling, hyperalgesia, allodynia, and hypoesthesia) will also be asked to the patients in the 1st month after surgery.
|
Chronic pain symptoms at 1st months
|
Pain scores at 3rd months
Time Frame: Chronic pain symptoms at 3rd months
|
Chronic pain symptoms will be assessed using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain).
Neuropathic pain symptoms (Burning, stabbing, electric shock-like pain, tingling, numbness, pins, and needles feeling, hyperalgesia, allodynia, and hypoesthesia) will also be asked to the patients in the 3rd month after surgery.
|
Chronic pain symptoms at 3rd months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Oya Kaybal, MD, Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2012-KAEK-15/2446
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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