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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03718377
Other study ID # 2018-06-006-002
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 28, 2018
Est. completion date June 2019

Study information

Verified date February 2019
Source Kyungpook National University
Contact Jimin Heo
Phone 82-53-420-5430
Email knuhmrc@knu.ac.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the effects of serratus plane block on intraoperative opioid consumption, emergence time and hemodynamic stability in patients undergoing video-assisted thoracic surgery.


Description:

Thoracotomy is known as one of the most painful surgery. Thus, there is a development to reduce surgical stress in terms of operation technique, which is video-assisted thoracoscopic surgery. Although it has reduced postoperative pain and complications compared with thoracotomy, VATS is still quite painful operation.

Serratus plane block is a novel technique which provide analgesic effect for lateral chest wall by blocking lateral branch of intercostal nerve. It has been reported to be used for pain management including rib fracture, herpes zoster, and postoperative pain. It has become a popular analgesic modality because it is easy to perform and relatively safe. However, the effect of serratus plane block during intraoperative period has not yet been studied.

In this study, therefore, the investigators decided to assess the effect of serratus plane block on intraoperative opioid consumption, emergence time and hemodynamic stability in patients undergoing video-assisted thoracic surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date June 2019
Est. primary completion date June 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

- American Society of Anesthesiologists physical status classification I-III for three port video-assisted thoracic surgery lobectomy under general anesthesia

Exclusion Criteria:

- History of allergic reaction to local anesthetics, coagulopathy, local infection at the injection site, and systemic infection.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Serratus plane block
The subjects were received serratus plane block in the regional-anesthesia unit out of operation room before induction of general anesthesia. And, video-assisted thoracic surgery was performed under balanced general anesthesia.
General anesthesia only
Video-assisted thoracic surgery was performed under balanced general anesthesia without serratus plane block

Locations

Country Name City State
Korea, Republic of Kyungpook national university hospital Daegu

Sponsors (1)

Lead Sponsor Collaborator
Kyungpook National University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intraoperative remifentanil consumption Intraoperative remifentanil consumption will be checked. through study completion, an average of 1 year
Secondary Emergence time Emergence time is duration between the end of surgery and extubation. Emergence time will be checked. through study completion, an average of 1 year
Secondary Systolic blood pressure Systolic blood pressure (mmHg) will be checked through study completion, an average of 1 year
Secondary Heart rate Heart rate (beats per minute) will be checked through study completion, an average of 1 year
Secondary Dose of rescue drugs used to control blood pressure and HR Dose of rescue drugs used to control blood pressure and HR will be checked through study completion, an average of 1 year
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