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Clinical Trials in Italy / NCT07586462
Recruiting Observational

Deep Rectus Sheath (DRS) Block in Abdominal Surgery

NCT07586462 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-05
Last updated
2026-05-22

Condition(s) studied

LaparoscopyAbdominal Surgery by Laparotomy

Investigational drug(s) / intervention(s)

Other blocks

Other blocks: Fascial plane blocks (TAP, QL, ESP, Rectus sheath)

Study summary

The goal of this observational study is to learn about the effectiveness of the Deep Rectus Sheath (Preperitoneal) block in patients undergoing abdominal surgery. The main question it aims to answer is:

Does the Deep Rectus Sheath block improve postoperative recovery and pain control compared to standard care or other fascial plane blocks in patients undergoing abdominal surgery?

Participants undergoing open or laparoscopic abdominal surgery as part of their routine clinical care will receive analgesic management according to standard practice, which may include systemic analgesia alone, Deep Rectus Sheath block, or other fascial plane blocks (such as TAP, ESP, or QL), depending on anesthesiologist choice. Postoperative outcomes will be collected prospectively, including quality of recovery (QoR-15 at 24 hours), pain scores at rest and during movement up to 48 hours, analgesic consumption, time to first analgesic request, mobilization time, and occurrence of complications.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Patients undergoing abdominal surgery, either open or laparoscopic * ASA physical status I-III * Neuraxial or general anesthesia according to standard clinical practice * Provision of informed consent to participate in the study Exclusion Criteria: * Refusal to provide informed consent * Contraindications to locoregional anesthesia * Known allergy to local anesthetic agents * Coagulation disorders or incompatible anticoagulant therapy * Infection at the injection site * Cognitive impairment preventing reliable assessment of outcomes

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Crotone Hospital Crotone Italy Not Yet Recruiting
Crotone Hospital Crotone Italy Recruiting

More San Giovanni di Dio Hospital trials in Italy

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07586462 on ClinicalTrials.gov ↗ ← All trials in Italy