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
- Diseases
- Colorectal cancer
- 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
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Asklepios Medical Center Uckermark Coordinator of this site? Confirm its status | Schwedt | Germany | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.