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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05700357
Other study ID # E.Kurul-E1-22-3143
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 28, 2022
Est. completion date December 28, 2024

Study information

Verified date February 2024
Source Ankara City Hospital Bilkent
Contact Emine N ZENGIN
Phone +905063370548
Email nilbavullu@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thoracotomy is one of the most painful operations known. Therefore, it causes severe acute pain. If pain is not controlled, it increases the frequency of postoperative pulmonary complications and postoperative morbidity. It can even cause chronic pain in the future. Thoracic epidural analgesia (TEA) is the gold standard method in the treatment of pain after thoracotomy. Thoracic paravertebral block (TPVB) is known as the most effective method after TEA. The fact that TPVB has fewer side effects than TEA increases the use of TPVB. There is no consensus on the dose of analgesia in studies. In the literature, volumes between 20 ml and 30 ml are frequently used for TPVB in recent years. This study, it was aimed to compare the efficacy of 20 ml, 25 ml, and 30 ml volumes of TPVB with local anesthetic at the same concentration (0.25% bupivacaine) on postoperative analgesia in patients undergoing thoracotomy.


Recruitment information / eligibility

Status Recruiting
Enrollment 75
Est. completion date December 28, 2024
Est. primary completion date November 28, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - 18 to 80 years old - American Society of Anesthesiologists (ASA) physical status I-II-III - BMI 18 to 40 kg/m2 - Elective thoracotomy surgery Exclusion Criteria: - Patient refusing the procedure - Emergency surgery - History of chronic opioid or analgesic used

Study Design


Intervention

Procedure:
TPVB with 20 ml
The thoracic paravertebral block will be applied to the patients with 20 ml of 0.25% bupivacaine under real-time ultrasound guidance.
TPVB with 25 ml
The thoracic paravertebral block will be applied to the patients with 25 ml of 0.25% bupivacaine under real-time ultrasound guidance.
TPVB with 30 ml
The thoracic paravertebral block will be applied to the patients with 30 ml of 0.25% bupivacaine under real-time ultrasound guidance.

Locations

Country Name City State
Turkey Ankara City Hospital Çankaya Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara City Hospital Bilkent

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Scores Pain will be assessed at the first-hour rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). 1st hour after surgery
Primary Pain Scores Pain will be assessed at the 2nd-hour rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). 2nd-hour after surgery
Primary Pain Scores Pain will be assessed at the 4th-hour rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). 4th-hour after surgery
Primary Pain Scores Pain will be assessed at the 12th-hour rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). 12th-hour after surgery.
Primary Pain Scores Pain will be assessed at the 24th-hour rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). 24th-hour after surgery.
Primary Pain Scores Pain will be assessed at the 48th-hour rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). 48th-hour after surgery.
Secondary Morphine Consumption Morphine consumption for 24 hours will be recorded 24 hours after surgery
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