Recruiting NCT05696002

Advanced Pelvic Surgical Oncology Database - Prospective Observational Study

— Observational Rectal Cancer Pelvic Cancer Gynecologic Cancer Colon Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to: Registry conditions: Rectal Cancer, Pelvic Cancer, Gynecologic Cancer, Colon Cancer. Basic parameters: No limits · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: United Kingdom
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Retrospective and prospective observational study of patients undergoing advanced pelvic oncological resection for maligancy including multi visceral resection, beyond TME resection and sacrectomy/flap reconstruction/urinary reconstruction at Glasgow Royal Infirmary. Goal is to study and report outcomes for patients to characterise and understand major complications, natural history of resectional patients and identify areas for future interventional study.

Detailed description

Goal is to study and report outcomes for patients to characterise and understand major complications, natural history of resectional patients and identify areas for future interventional study..

Primary outcome measures

Cancer-specific survival [Time frame: 10 years]
Overall survival [Time frame: 10 years]
Post-operative complications [Time frame: 10 years]
Quality of life (survey) [Time frame: 10 years]

Eligibility criteria

Inclusion criteria

Advanced pelvic oncological resection defined as more than 1 pelvic organ resected

Exclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model: Cohort

Study locations

United Kingdom · 1 center

Academic Department of Surgery, Glasgow Royal Infirmary — Glasgow

Identifiers

NCT: NCT05696002 · APSOD

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗