Incidence of Chronic Pain After Thoracic Surgery

Sponsor
Atatürk Chest Diseases and Chest Surgery Training and Research Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05145153
Collaborator
(none)
200
1
13
15.4

Study Details

Study Description

Brief Summary

Thoracotomy and video-assisted thoracic surgery procedures are frequently performed in thoracic surgery. It is widely accepted that thoracotomy causes severe acute pain. This prolongs the discharge time of the patients, and increases the frequency of postoperative pulmonary complications and postoperative morbidity. Postoperative acute pain may cause chronic thoracotomy pain in the later period, and may adversely affect the quality of life of the patients. Video-assisted thoracic surgery (VATS) has become the standard procedure in minor and major lung surgeries. Postoperative pain is seen in patients undergoing VATS, although it is not as severe as after thoracotomy. As in thoracotomy, this affects the postoperative pulmonary complications and the discharge time of the patients. Likewise, this pain can cause chronic pain.

In this study, it was aimed to analyze the symptoms of chronic pain in the 3rd and 6th months postoperatively in patients who had undergone thoracic surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Thoracic surgery application

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Incidence of Chronic Pain After Thoracic Surgery
Actual Study Start Date :
Sep 28, 2021
Anticipated Primary Completion Date :
Sep 28, 2022
Anticipated Study Completion Date :
Oct 28, 2022

Outcome Measures

Primary Outcome Measures

  1. Pain scores at 3th months. [Chronic pain symptoms at 3th months.]

    Choronic 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.

  2. Pain scores at 6th months. [Chronic pain symptoms at 6th months.]

    Choronic 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 6th month after surgery.

Secondary Outcome Measures

  1. Life quality [The effect of chronic pain on quality of life at 3rd and 6th months.]

    It will be questioned whether chronic pain affects the patient's quality of life. has no affect has little effect has medium affect has a lot of affects

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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 thoracic surgery

Exclusion Criteria:
  • Advanced cancer

  • History of chronic analgesic therapy

  • Patients with previous thoracic surgery

  • Patients who were operated under emergency conditions

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ankara Atatürk Chest Disease and Chest Surgery Training and Research Hospital Kecioren Ankara Turkey 06000

Sponsors and Collaborators

  • Atatürk Chest Diseases and Chest Surgery Training and Research Hospital

Investigators

  • Principal Investigator: Musa Zengin, MD, Atatürk Chest Diseases and Chest Surgery Training and Research Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Musa Zengin, Principal İnvestigator, Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT05145153
Other Study ID Numbers:
  • 2012-KAEK-15/2378
First Posted:
Dec 6, 2021
Last Update Posted:
Dec 6, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Musa Zengin, Principal İnvestigator, Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 6, 2021