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Search / Trial NCT06896578

Latitude - Lateral Lymph Node Attitude Study

Launched by SAHLGRENSKA UNIVERSITY HOSPITAL · Mar 19, 2025

Trial Information

Current as of May 09, 2025

Not yet recruiting

Keywords

Lateral Lymph Nodes Quality Of Life Local Recurrence Thrombosis Lymph Oedema Lateral Lymph Node Dissection

ClinConnect Summary

The Latitude study is looking at how to treat patients with advanced rectal cancer, specifically focusing on lymph nodes that might be affected by the tumor but are located outside the usual area that surgeons operate on. Some patients receive treatment before surgery, but there’s uncertainty about what to do if doctors still suspect these lymph nodes are affected. This study aims to figure out which lymph nodes should be removed during surgery and how this decision affects patients' cancer outcomes and their overall quality of life.

To participate in this trial, individuals need to be at least 18 years old and have a type of rectal cancer called adenocarcinoma, confirmed by a biopsy. They should have a tumor located a certain distance from the anal area and show evidence of lymph nodes that might be affected on imaging tests. Participants will need to provide written consent to join the study. This research is important because it could help doctors make better decisions about surgeries and improve the care and recovery of patients facing this challenging condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 18 years or older
  • written informed consent
  • adenocarcinoma verified tumour below ≤ 8 cm from anal verge measured by rectoscopy and/or MRI
  • clinical tumor (cT) stage cT3, cT4a or cT4b on MRI or
  • adenocarcinoma verified tumour at any height ≤ 15 cm from anal verge measured by rectoscopy and/or MRI regardless of T/N stage with visible lateral lymph node (according to definition 2.4.2) on pre-therapeutic MRI or PET-CT
  • Exclusion Criteria:
  • Not biopsy confirmed rectal cancer (adenocarcinoma)
  • Recurrent rectal cancer
  • Age below 18
  • Participation in other trials in conflict with the protocol and end-points of the Latitude study
  • No informed consent

About Sahlgrenska University Hospital

Sahlgrenska University Hospital, a leading healthcare institution in Sweden, is at the forefront of clinical research and innovation. Affiliated with the University of Gothenburg, the hospital integrates advanced medical care with cutting-edge research, facilitating a collaborative environment for scientific exploration and clinical trials. With a commitment to improving patient outcomes, Sahlgrenska University Hospital focuses on a wide range of therapeutic areas, leveraging its multidisciplinary expertise to advance healthcare solutions. The institution is dedicated to fostering ethical research practices and ensuring the highest standards of patient safety and care in all clinical trials.

Locations

Gothenburg, , Sweden

Patients applied

0 patients applied

Trial Officials

Eva Angenete, MD PhD

Principal Investigator

Sahlgrenska Universitetssjukhuset

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported