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Clinical Trials/NCT03240562
NCT03240562
Completed
Not Applicable

Ultrasound-guided Serratus Anterior Plane Block for Thoracic Surgery Pain?

Samsung Medical Center1 site in 1 country89 target enrollmentAugust 3, 2017

Overview

Phase
Not Applicable
Intervention
patient controlled analgesia
Conditions
Postoperative Pain
Sponsor
Samsung Medical Center
Enrollment
89
Locations
1
Primary Endpoint
opioid consumption
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The investigators aimed to assess Ultrasounde- guided serratus anterior plane block can be effective in acute postoperative pain following thoracic surgery.

Detailed Description

Analgesic options for thoracotomy are various with each having their own merits and demerits.Thoracic epidural is said to be the gold standard for management of thoracotomy pain. However, it is invasive procedure and many side effects. Other options include paravertebral block, interpleural block, intrathecal opioids. Especially, paravertebral block is thought good alternative to epidural anethesia. Most of these invasive neuraxial techniques demand normal coagulation parameters to be present. The serratus anterior plane block(SAPB) was done under ultrasound guidance in the mid-axillary line at the level of the fourth rib and the catheter was placed superficial to the serratus plane. The patient expressed relief in pain within 10 minutes of being given the bolus of local anaesthetic.Pain following thoracotomy is chiefly due to rib retraction, and damage to the serratus/intercostal muscles and intercostal nerves. A SAPB addresses both these aspects. SAPB has been mentioned in previous studies for management of rib fractures and breast surgeries. The investigators try to evaluate whether the SAPB is easy to perform and provides effective analgesia in patients undergoing thoracotomy with minimal side effects.

Registry
clinicaltrials.gov
Start Date
August 3, 2017
End Date
December 30, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • undergoing thoracic surgery (lobectomy or segmentectomy)

Exclusion Criteria

  • allergy to any drugs chronic pain disease with medication psychologic disorder anti-depressant drug chronic kidney disease ( Cr over 2.0 mg/dl) coagulopathy

Arms & Interventions

IV-PCA group

no block performing, only use intravenous patient controled analgesia(IV-PCA)

Intervention: patient controlled analgesia

SAPB group

serratus anterior plane block(SAPB) and intravenous patient controled analgesia(IV-PCA)

Intervention: serratus anterior plane block

SAPB group

serratus anterior plane block(SAPB) and intravenous patient controled analgesia(IV-PCA)

Intervention: patient controlled analgesia

Outcomes

Primary Outcomes

opioid consumption

Time Frame: the first 24hour in postoperative phase

the dose of PCA and residual opioid

Secondary Outcomes

  • postoperative pain scale(intraoperative(immediately after surgery), postoperative 6 ,12, 24 hour)
  • opioid consumption(the first 6,12 hour in postoperative phase)

Study Sites (1)

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