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Advanced Endoscopic Resections for Rectal Neoplasms

Adoption of Advanced Endoscopic Resection Methods in the Treatment of Rectal Neoplasms

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07410767
Enrollment
300
Registered
2026-02-13
Start date
2026-03-01
Completion date
2026-04-30
Last updated
2026-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal Adenocarcinoma, Rectal Adenoma, Rectal Cancer, Rectal Neuroendocrine Neoplasm, Recurrent Rectal Adenocarcinoma

Brief summary

This study evaluates how advanced endoscopic resection techniques affect treatment outcomes in adults with rectal cancer. Rectal cancer has traditionally been treated with standard abdominal surgery. Newer endoscopic techniques allow removal of selected early tumors and may reduce treatment-related complications. However, their effectiveness and safety in tumors with deeper invasion are not yet fully established. This multicenter retrospective observational study uses existing medical records from adults who underwent endoscopic or surgical resection of rectal tumors between 2015 and 2025. Researchers will analyze anonymized information on procedures performed and treatment outcomes to assess the safety and effectiveness of advanced endoscopic approaches. The results of this study may help guide treatment selection and improve care for people with rectal cancer.

Interventions

PROCEDUREEndoscopic submucosal dissection

Endoscopic submucosal dissection is an advanced endoscopic technique used to remove rectal tumors in one piece through the endoscope. A circumferential incision is then made in the mucosa, followed by careful dissection within the submucosal layer until the lesion is completely removed. This technique enables precise pathological assessment of tumor margins and depth of invasion and is typically used for lesions suspected to have superficial submucosal invasion without clear evidence of lymph node involvement. The procedure is performed using standard therapeutic endoscopic equipment and electrosurgical devices.

PROCEDUREEndoscopic intramuscular dissection

Endoscopic intermuscular dissection is an advanced endoscopic resection technique designed for rectal tumors with suspected deeper submucosal invasion. Following mucosal incision, the dissection is intentionally performed in the plane between the inner circular and outer longitudinal muscle layers of the rectal wall. This allows deeper en bloc tumor removal compared with conventional endoscopic submucosal dissection. The goal of this technique is to achieve complete resection while potentially avoiding radical surgery in selected patients. The procedure is performed endoscopically using specialized dissection knives and electrosurgical systems and requires advanced operator expertise.

Sponsors

Jagiellonian University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with rectal neoplasms treated by advanced endoscopic resection

Exclusion criteria

* hybrid resection performed * full-thickness resection performed * essential procedural or outcome data were unavailable

Design outcomes

Primary

MeasureTime frameDescription
Major intraprocedural bleeding rateDuring the procedureBleeding occurring during the procedure that required advanced endoscopic hemostatic interventions beyond standard coagulation with the tip of the knife of coagulation forceps, resulted in hemodynamic instability, caused a significant prolongation of the procedure over 15 minutes (based on video), or led to procedure interruption or conversion
Intraprocedural perforation rateDuring the procedureFull-thickness defect of the gastrointestinal wall identified during the procedure, evidenced by direct visualization of extraluminal structures (mesorectum or peritoneal cavity), or confirmed by the presence of free air on imaging performed immediately after the procedure.
Delayed bleeding rateWithin 28 days after the procedureSymptomatic bleeding including hematemesis, melena, or a hemoglobin decrease of more than 2 g/dL.
Delayed perforation rateWithin 14 days after the procedureClinical signs of peritonitis accompanied by radiological evidence of free intraperitoneal air.
Post-coagulation syndrome rateWithin 28 days following the procedureThe occurrence of localized abdominal pain or peritoneal irritation signs after EID, accompanied by inflammatory response (elevated white blood cell count or C-reactive protein), in the absence of radiological or endoscopic evidence of perforation.
The need for emergency interventionsWithin 30 days after the procedureAny unplanned therapeutic intervention related to the index procedure during hospitalization or follow-up, including repeat endoscopy, endoscopic or radiological intervention, blood transfusion, or surgical treatment. Planned surveillance procedures were not considered additional interventions.
Procedure-related mortality rateWithin 30 days after the procedureNumber of deaths occurring within 30 days of the index procedure that was directly attributable to the procedure or to procedure-related complications. Deaths unrelated to the procedure were reported but not considered procedure-related mortality.

Secondary

MeasureTime frameDescription
En bloc resection rateIntraproceduralThe rate of lesions removed in a single specimen, enabling accurate macroscopic and histological assessment as reported by an endoscopist in a procedure protocol.
Complete resection rateWithin 30 days after the procedureThe rate of lesions resected completely according to the pathological examination of the resected specimen.
Procedure timeIntraproceduralProcedure time was evaluated on the procedure video and defined as the interval from the insertion of the scope to its final withdrawal measured in minutes; anesthesia-related time was not included.
Length of hospital stayWithin 30 days after the procedureThe number of days from the day of the procedure (day 0) to the day of hospital discharge.
The need for additional treatmentWithin 12 months after the procedureThe number of patients who required completion surgery or adjuvant (chemo)radiotherapy.

Countries

Poland

Contacts

CONTACTZofia Orzeszko, MD
zofia.orzeszko@uj.edu.pl+123797145

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026