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Effect of Continue RISS Block in Thoracotomy

Not Applicable
Completed
Conditions
Thoracotomy
Postoperative Pain
Interventions
Other: IV PCA
Registration Number
NCT04443556
Lead Sponsor
Konya Meram State Hospital
Brief Summary

Thoracotomy is one of the most painful surgery. Acute postoperative pain increases postoperative morbidity and prolongs hospital stay and also may lead to developing a chronic pain syndrome. This study aimed to assess the efficacy of continuous rhomboid intercostal and subserratus plane (RISS) block by inserting a catheter under direct vision for controlling acute thoracotomy pain.

Detailed Description

Before the closure of the thoracotomy, the surgeon will place two catheters through a Tuohy needle into fascial planes for continue RISS block. First catheter tip will be place towards the interfascial planes between the rhomboid major and intercostal muscles and the second catheter tip will be place in subserratus fascial plane. Continue local anesthetics will be injected through the catheters for 48 hours.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Patients over 18 years of age undergoing elective thoracic surgery
  • American Society of Anesthesiologists (ASA) physical status I-III grade
Exclusion Criteria
  • Patient refusal
  • History of psychiatric and cognitive disorders.
  • Patients allergic to the drugs used in the study
  • Emergent surgery

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control GroupIV PCAStandart postoperative analgesia
Group Rhomboid Intercostal and Subserratus Plane BlockIV PCAStandart postoperative analgesia + Continue Rhomboid Intercostal and Subserratus Plane Block
Group Rhomboid Intercostal and Subserratus Plane BlockTramadolStandart postoperative analgesia + Continue Rhomboid Intercostal and Subserratus Plane Block
Primary Outcome Measures
NameTimeMethod
postoperative painpostoperative 48 hour

Numeric rating scale (NRS) NRS use numbers to rate pain from 0 (no pain) to 10 (worst pain).

Secondary Outcome Measures
NameTimeMethod
Analgesic consumptionPostoperative 48 hour

Total opioid consumption after the surgery

Trial Locations

Locations (1)

Konya Education and Training Hospital

🇹🇷

Konya, Turkey

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