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NCT07433140Completed

Effect of Rectus Block Timing on Opioid Use

The Effect of Timing of Rectus Sheath Blockade During Robotic Prostate Surgery on Opioid Consumption: A Randomized Double-Blind Study

Source: ClinicalTrials.gov · Last updated 3 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
50 (actual)
First submitted
23 Nov 2025
Start date
15 Mar 2026
Primary completion date
15 May 2026
Lead sponsor
Koc University Hospital
NCT number
NCT07433140

What you commit to

  • Study type: Interventional
  • Participants enrolled: 50
  • From 15 Mar 2026 to the primary completion date, 15 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous major abdominal/pelvic surgery

Other illness

  • History of significant psychiatric disorders
  • Patients who may have contraindications to nerve blocks (bleeding diathesis, infection, and local anesthetic allergy).

Age

  • \<18 years of age

Other

  • ASA (American Society of Anesthesiologists) IV, V patients
  • Non-elective emergency cases

Who the study is looking for

  • -ASA (American Society of Anesthesiologists) I-III adult patients with prostate cancer and benign prostate diseases scheduled for robotic surgery at Koç University Hospital.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Koc University Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.