NCT07900620Not yet recruiting
T1 Colorectal Cancer After Local Excision: Decision Between Surgery and Active Surveillance (T1LDA Trial)
Source: ClinicalTrials.gov · Last updated 28 Oct 2026
Brief summary (registry, in English)
The goal of this two-arm clinical trial is to compare additional surgery with active surveillance in patients with high-risk pT1 colorectal cancer after local excision. The main questions it aims to answer are Does additional surgery result in lower rates of distant or extraluminal recurrence compared with active surveillance? How do the two treatment strategies differ in survival, complications, quality of life, and treatment-related costs? Participants will be randomly assigned to either additional surgery or active surveillance. Patients assigned to the surgery group will undergo standard preoperative assessment followed by additional surgery. Following surgery, patients will undergo surveillance according to the predefined follow-up protocol. Patients assigned to the active surveillance group will not receive any additional treatment. They will undergo surveillance according to a more intensive predefined follow-up protocol.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- First submitted
- 12 Oct 2026
- Start date
- 1 Nov 2026
- Primary completion date
- 1 Nov 2032
- Lead sponsor
- Tampere University Hospital
- Diseases
- Colorectal cancer
- NCT number
- NCT07900620
What you commit to
- Study type: Interventional
- Planned participants: 500
- From 1 Nov 2026 to the primary completion date, 1 Nov 2032
- 14 sites in 1 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
- The patient is not eligible for either surgery or follow-up Multidisciplinary team (MDT) considers the surgical complication risk too high MDT considers the recurrence risk of surveillance strategy too high The patient is unable to understand information provided The patient is not willing to commit to the required follow-up
- R1 resection, defined as noncancerous margin \< 100 µm without cautery artefact and not meeting criteria for piecemeal resection
- History of previous CRC
Other illness
- Radiological involvement of lymph nodes (N+) in rectal cancer:
- Clearly pathologic nodes or suspicious nodes with additional risk factors, i.e. suspicious if: ≥9 mm or mucinous signal Smaller nodes 5-9 mm: Require 2 additional malignant features for cN+ classification. Nodes \<5 mm, unless mucinous, are considered benign.
- Additional malignant features: indistinct LN border or heterogeneous MRI signal
- Clear radiological suspicion of malignant lymph nodes in colon cancer size \>10 mm
- Actively treated invasive cancer within 2 years
- Any metastatic cancer
- Hereditary CRC syndrome
- Inflammatory bowel disease
Other
- Either no high-risk factors are present or four or more high-risk factors are present
- Radiological or histological EMVI+ (extramural vascular invasion) or radiological TD+ (tumor deposit)
- Suspected M1 level metastases
Who the study is looking for
- Histopathologically confirmed diagnosis of pT1 colorectal cancer
- Adenocarcinoma treated by endoscopic or transanal local excision
- One to three risk factors for LNM or recurrence present Lymphovascular invasion (LVI) Intermediate or high tumor budding (grade 2-3) Close margin resection, defined as 100-1000 µm histologically non-cancerous resection margin, measured from the closest part of invasive adenocarcinoma to the resection line, without direct adenocarcinoma involvement at the margin The histological margin cannot be reliably assessed due to cautery artifact at the resection margin, where carcinoma is present at the evaluable edge, reflecting the involvement of cancer in margin. However, given the endoscopist's impression of complete excision Piecemeal resection, where the endoscopist's impression is that complete excision has been achieved (unclear resection margin after an endoscopic resection reported to have good macroscopic margin, e.g. a successful piecemeal resection) Adenoma involvement of the resection margin defined as 0 µm WHO high-grade adenocarcinoma Perineural invasion DSI (\>1000µm invasion or Haggitt level 4 or Kudo sm3)
- Adequately performed primary colonoscopy, defined as a complete colonoscopy with visualization of the entire rectum and colon up to the cecum and no technical limitations compromising mucosal assessment or exclusion of synchronous disease
- Patient age 18 or more
- ECOG 0-2
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (14)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Kanta-Häme Central Hospital Coordinator of this site? Confirm its status | Hämeenlinna | Finland | Unknown status |
| North Carelia Central Hospital Coordinator of this site? Confirm its status | Joensuu | Finland | Unknown status |
| Jyväskylä Central Hospital Coordinator of this site? Confirm its status | Jyväskylä | Finland | Unknown status |
| Kymenlaakso Central Hospital Coordinator of this site? Confirm its status | Kotka | Finland | Unknown status |
| Kuopio University Hospital Coordinator of this site? Confirm its status | Kuopio | Finland | Unknown status |
| Päijät-Häme Central Hospital Coordinator of this site? Confirm its status | Lahti | Finland | Unknown status |
| Mikkeli Central Hospital Coordinator of this site? Confirm its status | Mikkeli | Finland | Unknown status |
| Oulu University Hospital Coordinator of this site? Confirm its status | Oulu | Finland | Unknown status |
| Satakunta Central Hospital Coordinator of this site? Confirm its status | Pori | Finland | Unknown status |
| Lapland Central Hospital Coordinator of this site? Confirm its status | Rovaniemi | Finland | Unknown status |
| Seinäjoki Central Hospital Coordinator of this site? Confirm its status | Seinäjoki | Finland | Unknown status |
| Tampere University Hospital Coordinator of this site? Confirm its status | Tampere | Finland | Unknown status |
| Turku University Hospital Coordinator of this site? Confirm its status | Turku | Finland | Unknown status |
| Vaasa Central Hospital Coordinator of this site? Confirm its status | Vaasa | Finland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.