Deep Rectus Sheath (DRS) Block in Abdominal Surgery
Recruiting
Observational Study
Laparoscopy
Abdominal Surgery by Laparotomy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Sex
- Any
- Study type
- Observational
- Participants needed
- 60 (estimated)
- Sponsor
- San Giovanni di Dio Hospital · Other
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About This Trial
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 un…
Trial Locations
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Eligibility Criteria
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…
Contacts