NCT06061432Not yet recruiting
Endoscopic Ultrasound- Guided Hartmann Reversal Procedure
Endoscopic Reconstruction of the Gastrointestinal Tract After Surgical Resection Procedures Within the Large Intestine (Hartmann's Procedure- Modification of the Method Facilitating the Restoration of Gastrointestinal Continuity)
Source: ClinicalTrials.gov · Last updated 29 Sept 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The goal of this clinical trial is to learn about clinical usefulness endoscopic gastrointestinal anastomoses to restore the gastrointestinal continuity in patients with permanent colostomy after Hartmann procedure. The main questions it aims to answer are: * is the endoscopic restore the gastrointestinal continuity procedure effective? * is this endoscopic procedure safe?
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 12 Sept 2023
- Start date
- 1 Dec 2023
- Primary completion date
- 31 Dec 2024
- Lead sponsor
- Nicolaus Copernicus University
- Diseases
- Colorectal cancer
- NCT number
- NCT06061432
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 1 Dec 2023 to the primary completion date, 31 Dec 2024
- No sites listed in no 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
- participants ineligible for surgery
Other illness
- allergy to any of the materials used in the study
- participants with advanced cancer in the metastatic stage
Other
- pregnancy, breastfeeding, or intention to become pregnant during the study
- contraindications to electrosurgical instruments
- participants ineligible for restoration of gastrointestinal continuity
- participants ineligible for general anesthesia
Who the study is looking for
- participants of both sexes aged above 18 years
- participants, who provided informed consent for such treatment
- eligibility for Hartmann's procedure according to current medical knowledge based on evidence-based medicine.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.