Clin2
NCT05476263Possibly a fitRecruiting

Negative pressure wound therapy for esophagus or rectum

Esophagus InjuryRectal Lesion

Part of Digestive system, Injuries & trauma clinical trials.

This trial studies whether a device called Suprasorb CNPendo helps healing of certain full-thickness (through-and-through) injuries or wounds in the esophagus or rectum. It may be an option if your medical team is already considering negative pressure wound therapy for these specific problems.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
110 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years or older.
  • You have an acute (new) full-thickness defect or injury/wound in your esophagus or rectum, such as a perforation or an anastomotic leak.
  • Your doctor believes the Suprasorb CNPendo treatment is appropriate for your situation based on the device instructions (IFU) and medical guidelines.
  • You can sign informed consent to allow the study to use your data.
  • You do not have a known bleeding/clotting problem that raises your bleeding risk.
  • Your wound does not involve the breathing tubes (trachea/bronchus/lungs), and you are able to follow the device instructions as planned.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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