Colon CancerSENTRYNCT06652672
Sentinel Node and Organ-sparing Surgery in Stage I Colon Carcinoma
A study testing Organ-sparing surgery in people with Colon Cancer and Colon Adenocarcinoma, run by Meander Medical Center at 1 site in Netherlands.
Trial summary
The aim of this study is to reduce the need for colectomy and its' associated morbidity and mortality in patients with pT1-2 colon carcinoma after endoscopic resection and an estimated lymph node metastasis (LNM) risk of >15%, or with macroscopically suspected T1 tumors, by performing an endoscopic-assisted… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Colon Cancer, Colon Adenocarcinoma, Sentinel Lymph Node
- What is being tested?
- Organ-sparing surgery
- Type of treatment
- Injection or infusion, Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 341 participants
- Where
- 1 siteNetherlands
- Study dates
- 12 Dec 2024to 12 Dec 2032
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Oral and written informed consent (IC)
- Aged 18 years and older
- Fit for both organ-sparing surgery and colectomy
- Pathologically confirmed T1-2 adenocarcinoma of the colon following R0, R1, or Rx endoscopic resection with an estimated LNM risk >15% (Table 5.2.2. in module 5.2 of the Dutch CRC guideline); or a lesion macroscopically suspected to be (deep-invasive) T1 colon cancer, measuring <40 mm, for which wedge resection is considered the most suitable local resection technique as recommended by the MDT
- The resection scar after local excision is expected to be clearly recognized at endoscopy, either by a tattoo or by detecting a scar in the colorectal segment where no other polypectomies were performed
- Lesion located >25cm from the anus based on endoscopic measurement, or above sigmoid take-off
Who cannot join
- Patients who opt for active follow-up instead of surgery following shared decision-making
- Distant metastasis
- Lynch syndrome
- Another active malignancy requiring palliative treatment at the time of colon cancer diagnosis
- Previous colorectal cancer within the last 5 years
- Tumours that comprised >50% of the colon circumference before resection
Show all 13Show fewer
- Tumours involving the ileocaecal valve
- Pregnancy, lactation or a planned pregnancy during the course of the study
- Known allergy to any of the compounds used for SLN identification (ICG, Iodine or Sodium iodide)
- Previous colonic surgery (excluding appendectomy)
- Contra-indication for laparoscopic or robotic surgery
- Severe kidney- or liver failure
- Hyperthyroidism or an autonomously functioning thyroid adenoma
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Netherlands1 site, 1 recruiting
- Recruiting
Meander Medisch Centrum
Amersfoort
Bart CT van de Laar, MD, +31338507137, bct.vande.laar@meandermc.nl
About this study
Official title: Sentinel Node and Organ-sparing Surgery in Stage I Colon Carcinoma (SENTRY Trial)
The aim of this study is to reduce the need for colectomy and its' associated morbidity and mortality in patients with pT1-2 colon carcinoma after endoscopic resection and an estimated lymph node metastasis (LNM) risk of >15%, or with macroscopically suspected T1 tumors, by performing an endoscopic-assisted laparoscopic/robotic wedge resection of the tumor or scar, along with sentinel node (SLN) biopsy using indocyanine green (ICG). This intervention will be compared to the standard-of-care segmental resection using a partially randomized patient preference design. The primary outcome is the 3-year recurrence rate.
Read the detailed description
Colorectal cancer is the third most common type of cancer in the Netherlands and the second leading cause of cancer-related deaths. An increased incidence of T1-2 tumors has been observed following the introduction of population screening programs, leading to more frequent endoscopic excisions. The risk of LNM in T1-2 colon cancers is relatively low. However, local excision does not allow assessment of lymph node status. Moreover, the diagnostic accuracy of computed tomography (CT) and other preoperative imaging modalities for detecting LNM remains limited.
Segmental colonic resections are associated with substantial morbidity. Based on large population-based datasets, 33% of patients experience at least one complication, including anastomotic leakage, with a postoperative mortality rate of 1.5-3.1%. Morbidity is known to substantially impact quality of life and contribute to a high economic burden. Additionally, major symptoms of low anterior resection syndrome (LARS) are present in 21% of patients after segmental resection, with reported effects on quality of life comparable to those experienced by patients who undergo rectal cancer resection and develop LARS.
To minimize unnecessary completion surgery, histopathological risk stratification is applied. In the Netherlands, histopathological risk factors for the presence of LNM in pT1-2 colon cancer are poor (high-grade) differentiation, lymphovascular invasion, high-grade tumor budding (Bd 2-3), and Haggitt level 4. The risk of LNM varies depending on the number of risk factors, pT stage, polyp morphology, and margin status. Completion segmental resection is omitted for pT1-2 tumors with a predicted LNM risk below 15%. Management is guided by risk stratification: for a 5-15% risk, active follow-up is preferred; for a 15-25% risk, active follow-up may be considered as an alternative to completion segmental resection through shared decision-making; and for a >25% risk, segmental resection is the preferred treatment. However, the vast majority of patients with a >15% risk of LNM who undergo surgery experience potential harm but no benefit, as they ultimately do not have LNM. Additionally, suspected T1 tumors are sometimes difficult or impossible to resect endoscopically. In such cases, wedge resection or segmental resection is the standard of care. Depending on T stage and other histopathological risk factors identified after wedge resection, a subsequent segmental resection may still be required. By adding SLN biopsy to the procedure, we aim to avoid the need for segmental resection after wedge resection.
The investigators hypothesize that, in patients who have undergone R0/R1/Rx endoscopic resection of T1-2 colon cancer and have a >15% risk of LNM, or in those with macroscopically suspected T1 tumors, an SLN biopsy combined with wedge resection of the residual tumor or scar can safely spare the majority of patients with negative SLNs from undergoing segmental resection. In our systematic review and meta-analysis, we found a pooled accuracy of 98% and a sensitivity of 80% for SLN detection in T1-2 colon cancer. The investigators use endoscopic submucosal injection of ICG at the tumor site, which carries a low risk of intra-abdominal spillage that could hinder SLN identification.
The SLN biopsy will be combined with an endoscopy-assisted wedge resection of the tumor or scar following endoscopic resection. During the endoscopy-assisted wedge resection, the surgeon first identifies and mobilizes the colon to facilitate the wedge resection. A gastroenterologist then performs a colonoscopy to visualize the scar from the previously resected tumor. With intraluminal endoscopic visualization, the surgeon places a suture to provide traction and position the linear stapler. The gastroenterologist confirms complete inclusion of the scar and ensures lumen patency before the stapler is fired. Endoscopy-assisted limited wedge resection is associated with low complication rates and is performed at lower cost compared to laparoscopic segmental resection. Because no anastomosis is created, the risk of anastomotic leakage is eliminated. This approach could reduce morbidity, mortality, hospital stay, and stoma rates. Although staple line failure and leakage are theoretical risks, such complications have not been reported in previous cases.
Patients with a positive SLN (macro- or micrometastasis) or T3-4 tumors are offered segmental resection. Node-positive patients are recommended to undergo adjuvant chemotherapy if performance status allows. SLN-negative patients do not undergo further surgery and are managed with an intensive follow-up strategy. Assuming 80% sensitivity and a 20% prevalence of lymph node metastasis, the risk of retained positive nodes after SLN biopsy is approximately 4%. Additionally, tumor deposits (TDs) could potentially be missed when patients are treated with SLN biopsy and wedge resection. However, only 0.45% of patients with stage I disease are TD-positive. The investigators consider the absolute risks of missed lymph node metastases and TDs acceptable, given the reduced perioperative morbidity and mortality associated with segmental resection.
The SENTRY trial will be the first to offer organ-sparing surgery combined with an SLN biopsy for patients with selected early-stage colon cancer. This organ-sparing approach is anticipated to improve postoperative mortality, morbidity, hospital stay, quality of life, and costs compared to standard segmental resection, without compromising oncologic outcomes. This multicenter, partially randomized, patient-preference trial will compare the organ-sparing approach with standard-of-care segmental resection to assess oncologic safety.
- Conditions
- Colon Cancer, Colon Adenocarcinoma, Sentinel Lymph Node, Sentinel Lymph Node Biopsy, Colon Neoplasms, Colon Neoplasm
- Being tested
- Organ-sparing surgery, Standard of care segmental resection
- Keywords
- Colon cancer, Fluorescence, Sentinel lymph node, Indocyanine green (ICG), Organ sparing surgery, Organ preserving surgery, Local resection
- Medical subject headings
- Colonic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Organ-sparing surgeryProcedure or surgery
Endoscopy-assisted laparoscopic/robotic wedge resection and sentinel lymph node biopsy using submucosal injection of ICG.
Standard of care segmental resectionProcedure or surgery
Standard of care segmental resection of the affected part of the colon including removal of regional lymph nodes.
| Study group | Role | What they receive |
|---|---|---|
| Organ-sparing surgery | Experimental | Local resection with sentinel lymph node biopsy Receives: Procedure: Organ-sparing surgery |
| Standard of care segmental resection | Active comparator | Not described Receives: Procedure: Standard of care segmental resection |
What is being measured
The primary outcome is the main question the study is designed to answer.
3-year recurrence rate
Measured: 3 years postoperatively
Successful sentinel lymph node biopsy
Percentage of patients undergoing a successful sentinel lymph node biopsy with one or more sentinel lymph nodes detected
Measured: Intraoperative
Secondary outcomes (19)
5-year recurrence rate
Measured: 5 years postoperatively
3-year overall survival
Measured: 3 years postoperatively
5-year overall survival
Measured: 5 years after postoperatively
90-days complication rate
Clavien-Dindo classification
Measured: 90 days postoperatively
90-days postoperative mortality
Measured: 90 days postoperatively
Proportion of patients with preference for standard and experimental treatment, and without preference
Measured: 1 day postoperatively
Procedure time of organ-sparing surgery and segmental resection
Measured: Directly after surgery, on the same day
Successful wedge resections
Percentage of patients undergoing a successful wedge resection
Measured: Intraoperative
Intraoperative complications
Measured: Intraoperative
Upstaging of sentinel lymph nodes due to ultrastaging
If sentinel lymph nodes test negative after routine HE staining, ultrastaging is performed. During this process, the lymph nodes are sectioned at 200 µm intervals and examined at three levels using HE staining, as well as immunohistochemistry for cytokeratin AE1/AE3. Sentinel lymph nodes are considered upstaged if they are initially negative on HE staining but are positive during ultrastaging, either with macrometastases (>2 mm) or micrometastases (0.2-2 mm).
Measured: During postoperative pathological examination, conducted within two weeks after surgery.
Quality of life - EQ5D-5L
EuroQoL 5-Dimension 5-Level. Range 1-5 per dimension. Higher means worse quality of life.
Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively
Quality of life - QLQ-CR29
QLQ-CR29 questionnaire: Organisation for Research and Treatment of Cancer (EORTC) colorectal quality of life module QLQ-CR29. Range 0-100. Higher scores indicate higher levels of symptoms or less functioning.
Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24 months postoperatively.
Quality of life - QLQ-C30
European Organization for Research and Treatment (EORTC) quality of life questionnaire (QLQ-C30): Range 0-100. A high score on each scale represents a high level in the examined topic, a high score on the global health status for instance represents a high quality of life and a high score in a symptom scale represents a high level of symptoms/problems.
Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24 months postoperatively.
Quality of life - Surv100
Surv100 questionnaire: European Organization for Research and Treatment (EORTC) quality of life questionnaire survivorship (Surv100). 100 items on a 4- or 7-point Likert scale. A high score on each scale represents a high level in the examined topic, a high score on the global health status for instance represents a high quality of life and a high score in a symptom scale represents a high level of symptoms/problems.
Measured: From enrollment to the end of study. Questionnaires will be sent 36, 48, and 60 months postoperatively
Quality of life - LARS
LARS questionnaire: Low Anterior Resection Syndrome (LARS) score. 0-20 points, no LARS; 21-29 points, minor LARS; 30-42 points, major LARS.
Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively
Quality of life - WAI
WAI questionnaire: Work Ability Index. Range 7-49. The total WAI scores are categorized into 4 levels: poor (7-27), moderate (28-36), good (37-43), and excellent (44-49).
Measured: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively
Quality of life - iMCQ
iMTA Medical Consumption Questionnaire (iMCQ): The iMCQ includes questions related to frequently occurring contacts with health care providers.
Measured: From enrollment to the end of study. Questionnaires will be sent 6, 12, 18, and 24 months postoperatively
Costs associated with wedge resection and sentinel lymph node biopsy.
Bottom-up micro costing will be applied.
Measured: 5 years postoperatively
Costs standard of care segmental resection
Bottom-up micro costing will be applied.
Measured: 5 years postoperatively
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Oct 2024
- Study start12 Dec 2024
- Primary completion12 Dec 2030 (estimated)
- Study completion12 Dec 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Colon CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- Multi-center, prospective, non-inferior, partially randomized patient-preference trial
- Masking
- None (open label)
- Enrolment
- 341 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Meander Medical Center
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Esther Consten, Meander Medical Center
- Investigators
- Frank J Voskens, Principal investigator, Meander Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06652672
- Sponsor's protocol ID
- NL84875.100.23
- Other IDs
- NL84875.100.23
- Acronym
- SENTRY
- Status last verified
- Nov 2025
- First submitted
- 8 Oct 2024
- Last updated
- 20 Nov 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Sentinel Node and Organ-sparing Surgery in Stage I Colon Carcinoma (SENTRY Trial)
- ClinicalTrials.gov ID
- NCT06652672
- Acronym / sponsor ID
- SENTRY / NL84875.100.23
- Conditions
- Colon Cancer, Colon Adenocarcinoma, Sentinel Lymph Node, Sentinel Lymph Node Biopsy, Colon Neoplasms, Colon Neoplasm
- Keywords
- Colon cancer, Fluorescence, Sentinel lymph node, Indocyanine green (ICG), Organ sparing surgery, Organ preserving surgery, Local resection
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 341 participants (estimated)
- Lead sponsor
- Meander Medical CenterUniversity, hospital or other
- Study start
- 12 Dec 2024 (actual)
- Primary completion
- 12 Dec 2030 (estimated)
- Study completion
- 12 Dec 2032 (estimated)
- First posted
- 22 Oct 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to reduce the need for colectomy and its' associated morbidity and mortality in patients with pT1-2 colon carcinoma after endoscopic resection and an estimated lymph node metastasis (LNM) risk of >15%, or with macroscopically suspected T1 tumors, by performing an endoscopic-assisted laparoscopic/robotic wedge resection of the tumor or scar, along with sentinel node (SLN) biopsy using indocyanine green (ICG). This intervention will be compared to the standard-of-care segmental resection using a partially randomized patient preference design. The primary outcome is the 3-year recurrence rate.
Detailed description
Colorectal cancer is the third most common type of cancer in the Netherlands and the second leading cause of cancer-related deaths. An increased incidence of T1-2 tumors has been observed following the introduction of population screening programs, leading to more frequent endoscopic excisions. The risk of LNM in T1-2 colon cancers is relatively low. However, local excision does not allow assessment of lymph node status. Moreover, the diagnostic accuracy of computed tomography (CT) and other preoperative imaging modalities for detecting LNM remains limited.
Segmental colonic resections are associated with substantial morbidity. Based on large population-based datasets, 33% of patients experience at least one complication, including anastomotic leakage, with a postoperative mortality rate of 1.5-3.1%. Morbidity is known to substantially impact quality of life and contribute to a high economic burden. Additionally, major symptoms of low anterior resection syndrome (LARS) are present in 21% of patients after segmental resection, with reported effects on quality of life comparable to those experienced by patients who undergo rectal cancer resection and develop LARS.
To minimize unnecessary completion surgery, histopathological risk stratification is applied. In the Netherlands, histopathological risk factors for the presence of LNM in pT1-2 colon cancer are poor (high-grade) differentiation, lymphovascular invasion, high-grade tumor budding (Bd 2-3), and Haggitt level 4. The risk of LNM varies depending on the number of risk factors, pT stage, polyp morphology, and margin status. Completion segmental resection is omitted for pT1-2 tumors with a predicted LNM risk below 15%. Management is guided by risk stratification: for a 5-15% risk, active follow-up is preferred; for a 15-25% risk, active follow-up may be considered as an alternative to completion segmental resection through shared decision-making; and for a >25% risk, segmental resection is the preferred treatment. However, the vast majority of patients with a >15% risk of LNM who undergo surgery experience potential harm but no benefit, as they ultimately do not have LNM. Additionally, suspected T1 tumors are sometimes difficult or impossible to resect endoscopically. In such cases, wedge resection or segmental resection is the standard of care. Depending on T stage and other histopathological risk factors identified after wedge resection, a subsequent segmental resection may still be required. By adding SLN biopsy to the procedure, we aim to avoid the need for segmental resection after wedge resection.
The investigators hypothesize that, in patients who have undergone R0/R1/Rx endoscopic resection of T1-2 colon cancer and have a >15% risk of LNM, or in those with macroscopically suspected T1 tumors, an SLN biopsy combined with wedge resection of the residual tumor or scar can safely spare the majority of patients with negative SLNs from undergoing segmental resection. In our systematic review and meta-analysis, we found a pooled accuracy of 98% and a sensitivity of 80% for SLN detection in T1-2 colon cancer. The investigators use endoscopic submucosal injection of ICG at the tumor site, which carries a low risk of intra-abdominal spillage that could hinder SLN identification.
The SLN biopsy will be combined with an endoscopy-assisted wedge resection of the tumor or scar following endoscopic resection. During the endoscopy-assisted wedge resection, the surgeon first identifies and mobilizes the colon to facilitate the wedge resection. A gastroenterologist then performs a colonoscopy to visualize the scar from the previously resected tumor. With intraluminal endoscopic visualization, the surgeon places a suture to provide traction and position the linear stapler. The gastroenterologist confirms complete inclusion of the scar and ensures lumen patency before the stapler is fired. Endoscopy-assisted limited wedge resection is associated with low complication rates and is performed at lower cost compared to laparoscopic segmental resection. Because no anastomosis is created, the risk of anastomotic leakage is eliminated. This approach could reduce morbidity, mortality, hospital stay, and stoma rates. Although staple line failure and leakage are theoretical risks, such complications have not been reported in previous cases.
Patients with a positive SLN (macro- or micrometastasis) or T3-4 tumors are offered segmental resection. Node-positive patients are recommended to undergo adjuvant chemotherapy if performance status allows. SLN-negative patients do not undergo further surgery and are managed with an intensive follow-up strategy. Assuming 80% sensitivity and a 20% prevalence of lymph node metastasis, the risk of retained positive nodes after SLN biopsy is approximately 4%. Additionally, tumor deposits (TDs) could potentially be missed when patients are treated with SLN biopsy and wedge resection. However, only 0.45% of patients with stage I disease are TD-positive. The investigators consider the absolute risks of missed lymph node metastases and TDs acceptable, given the reduced perioperative morbidity and mortality associated with segmental resection.
The SENTRY trial will be the first to offer organ-sparing surgery combined with an SLN biopsy for patients with selected early-stage colon cancer. This organ-sparing approach is anticipated to improve postoperative mortality, morbidity, hospital stay, quality of life, and costs compared to standard segmental resection, without compromising oncologic outcomes. This multicenter, partially randomized, patient-preference trial will compare the organ-sparing approach with standard-of-care segmental resection to assess oncologic safety.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Multi-center, prospective, non-inferior, partially randomized patient-preference trial
| Arm | Type | Receives |
|---|---|---|
| Organ-sparing surgery | Experimental | Procedure: Organ-sparing surgeryLocal resection with sentinel lymph node biopsy |
| Standard of care segmental resection | Active comparator | Procedure: Standard of care segmental resection |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Oral and written informed consent (IC)
- Aged 18 years and older
- Fit for both organ-sparing surgery and colectomy
- Pathologically confirmed T1-2 adenocarcinoma of the colon following R0, R1, or Rx endoscopic resection with an estimated LNM risk >15% (Table 5.2.2. in module 5.2 of the Dutch CRC guideline); or a lesion macroscopically suspected to be (deep-invasive) T1 colon cancer, measuring <40 mm, for which wedge resection is considered the most suitable local resection technique as recommended by the MDT
- The resection scar after local excision is expected to be clearly recognized at endoscopy, either by a tattoo or by detecting a scar in the colorectal segment where no other polypectomies were performed
Key exclusion criteria (13 listed)
- Patients who opt for active follow-up instead of surgery following shared decision-making
- Distant metastasis
- Lynch syndrome
- Another active malignancy requiring palliative treatment at the time of colon cancer diagnosis
- Previous colorectal cancer within the last 5 years
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Organ-sparing surgeryEndoscopy-assisted laparoscopic/robotic wedge resection and sentinel lymph node biopsy using submucosal injection of ICG. | Procedure or surgery | Organ-sparing surgery |
| Standard of care segmental resectionStandard of care segmental resection of the affected part of the colon including removal of regional lymph nodes. | Procedure or surgery | Standard of care segmental resection |
Primary outcome
3-year recurrence rate
Time frame: 3 years postoperatively
Successful sentinel lymph node biopsy
Time frame: Intraoperative
Percentage of patients undergoing a successful sentinel lymph node biopsy with one or more sentinel lymph nodes detected
19 secondary outcomes
5-year recurrence rate
Time frame: 5 years postoperatively
3-year overall survival
Time frame: 3 years postoperatively
5-year overall survival
Time frame: 5 years after postoperatively
90-days complication rate
Time frame: 90 days postoperatively
90-days postoperative mortality
Time frame: 90 days postoperatively
Proportion of patients with preference for standard and experimental treatment, and without preference
Time frame: 1 day postoperatively
Procedure time of organ-sparing surgery and segmental resection
Time frame: Directly after surgery, on the same day
Successful wedge resections
Time frame: Intraoperative
Intraoperative complications
Time frame: Intraoperative
Upstaging of sentinel lymph nodes due to ultrastaging
Time frame: During postoperative pathological examination, conducted within two weeks after surgery.
Quality of life - EQ5D-5L
Time frame: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively
Quality of life - QLQ-CR29
Time frame: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24 months postoperatively.
Quality of life - QLQ-C30
Time frame: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24 months postoperatively.
Quality of life - Surv100
Time frame: From enrollment to the end of study. Questionnaires will be sent 36, 48, and 60 months postoperatively
Quality of life - LARS
Time frame: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively
Quality of life - WAI
Time frame: From enrollment to the end of study. Questionnaires will be sent preoperatively and 6, 12, 18, 24, 36, 48, and 60 months postoperatively
Quality of life - iMCQ
Time frame: From enrollment to the end of study. Questionnaires will be sent 6, 12, 18, and 24 months postoperatively
Costs associated with wedge resection and sentinel lymph node biopsy.
Time frame: 5 years postoperatively
Costs standard of care segmental resection
Time frame: 5 years postoperatively
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Nov 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Frank J Voskens principal investigator
Meander Medical Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Organ-sparing surgery in people with Colon Cancer and Colon Adenocarcinoma, run by Meander Medical Center at 1 site in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 20 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Bart CT van de Laar (+31338507137, bct.vande.laar@meandermc.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
3-year recurrence rate (time frame: 3 years postoperatively). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Nov 2025.