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NCT07099924Recruiting

Rectus Sheath Catheters Following Midline Laparotomy

Bilateral Rectus Sheath Catheters Following Midline Laparotomy. A Randomized, Placebo-controlled Trial

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

Rectus sheath catheters (RSC) are used for postoperative analgesia following midline laparotomies. Local anesthetics are applied to the posterior rectus sheath via the RSC. The target structures are the anterior cutaneous branches of the spinal nerves Th7-Th12. RSC can be used in particular if thoracic epidurals are contraindicated (compromised coagulation), technically unfeasible or refused by the patient. The study investigates placebo-controlled weather RSC have a significant additional analgesic effect in a multimodal analgesic concept. Primary outcome parameters are the maximum pain score, the Quality-of-Recovery-15-Score (QoR-15GE) and the opioid consumption (morphine equivalents) in the first 72h postoperatively.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
16 Jul 2025
Start date
6 Oct 2025
Primary completion date
Aug 2027
Lead sponsor
Asklepios Kliniken Hamburg GmbH
NCT number
NCT07099924

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 6 Oct 2025 to the primary completion date, Aug 2027
  • 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

  • drug addiction
  • post-operative ventilation that cannot be completed on the day of surgery

Other illness

  • known allergy to local anesthetics used
  • chronic pain syndrome

Other

  • Local signs of inflammation
  • lack of consent or cooperation
  • pregnancy
  • participation in another medical study
  • sepsis

Who the study is looking for

  • Median laparotomy
  • Age over 18 years
  • Informed consent has been obtained

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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Asklepios Medical Center Uckermark
Coordinator of this site? Confirm its status
SchwedtGermanyRecruiting

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