Koc University Hospital
Istanbul, 34010, Turkey (Türkiye)
NCT Number: NCT07433140
The aim of this study is to observe the effect of administering local anesthetic to the abdominal wall at the beginning or end of surgery under general anesthesia on opioid consumption during surgery. The hypothesis of this study is to demonstrate that administering a rectus sheath block before the surgical procedure under general anesthesia is effective in reducing intraoperative opioid consumption and opioid-related side effects compared to administering it after the surgery is completed.
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Notify Me18 year and older
Male
Interventional
Not applicable
Istanbul, 34010, Turkey (Türkiye)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
-ASA (American Society of Anesthesiologists) I-III adult patients with prostate cancer and benign prostate diseases scheduled for robotic surgery at Koç University Hospital.
Exclusion criteria
Bilateral rectus sheat block will be performed after the anesthesia induction, before the start of the surgery
Bilateral rectus sheat block will be performed after the completion of the surgery, before the end of general anesthesia
Time frame: Total operative duration
Time frame: Total operative duration
Total intraoperative remifentail consumption divided by the weight of the patient (kg) and total operative duration (minutes). (mcg/kg/dk)
Time frame: From the end of the surgery to the end of the first postoperative hour
Cumulative opioid consumption at postoperative 1st hour in IV morphine equivalent
Time frame: From the end of the surgery to the end of the 6th postoperative hour
Cumulative opioid consumption at postoperative 6th hour in IV morphine equivalent
Time frame: From the end of the surgery to the end of the 12th postoperative hour
Cumulative opioid consumption at postoperative 12th hour in IV morphine equivalent
Time frame: From the end of the surgery to the end of the 24th postoperative hour
Cumulative opioid consumption at postoperative 24th hour in IV morphine equivalent
Time frame: At the end of the postoperative 1st hour
Pain measured by Numeric Rating Scale (0-10)
Time frame: At the end of the postoperative 6th hour
Pain measured by Numeric Rating Scale (0-10)
Time frame: At the end of the postoperative 12th hour
Pain measured by Numeric Rating Scale (0-10)
Time frame: At the end of the postoperative 24th hour
Pain measured by Numeric Rating Scale (0-10)
Time frame: From the end of the surgery to the end of the first postoperative hour
Total rescue fentanyl administered (mcg)
Time frame: At the end of the 24th postoperative hour
Patient satisfaction reported by the patient in a scale from 1 to 5
Koc University Hospital
Other
The Effect of Timing of Rectus Sheath Blockade During Robotic Prostate Surgery on Opioid Consumption: A Randomized Double-Blind Study
Acronym: PROSTIMERSBOP
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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