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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05145153
Other study ID # 2012-KAEK-15/2378
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 28, 2021
Est. completion date November 28, 2024

Study information

Verified date May 2024
Source Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Contact Musa Zengin, MD
Phone 903125677233
Email musazengin@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date November 28, 2024
Est. primary completion date October 8, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Thoracic surgery application
The chronic pain findings of the patients who underwent thoracic surgery will be questioned at the postoperative 3rd and 6th months.

Locations

Country Name City State
Turkey Ankara Atatürk Chest Disease and Chest Surgery Training and Research Hospital Kecioren Ankara

Sponsors (1)

Lead Sponsor Collaborator
Atatürk Chest Diseases and Chest Surgery Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain scores 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. Chronic pain symptoms at 3th months.
Primary Pain scores 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. Chronic pain symptoms at 6th months.
Secondary Life quality 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
The effect of chronic pain on quality of life at 3rd and 6th months.
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