Prostate Cancer Trial, Recruiting NCT06691776 Sponsor: The Netherlands Cancer Institute Condition: Prostate Cancer
Back to Prostate Cancer

Prostate Cancer Trial, Recruiting

NCT06691776
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

General requirements (all groups):

  • Adults aged 18 or older who have been referred for a radiotherapy treatment plan that matches one of the specific cancer groups in the trial
  • People with a general health and activity level that falls within a certain range (rated 0–3 on a standard medical scale, where 0 means fully active and 3 means limited self-care ability)
  • People who have signed and dated a consent form before any study procedures begin

Prostate cancer group:

  • People approved for radiotherapy to the prostate and nearby pelvic lymph nodes
  • People with prostate cancer confirmed by a tissue sample (biopsy)
  • People whose cancer has been assessed as a certain stage based on tumour size and spread (cT1–4)
  • People where cancer has been found in nearby lymph nodes, confirmed by a specialised scan (PSMA-PET/CT) or by a surgical procedure
  • People where no distant spread has been found on a PSMA-PET/CT scan, or those with limited distant spread who are still being considered for local radiotherapy

Cervical cancer group:

  • People approved for radiotherapy to the cervix and pelvic lymph nodes (25 treatment sessions, followed by an additional targeted radiation boost)
  • People with cervical cancer confirmed by a tissue sample
  • People whose cancer falls within certain staging categories (FIGO IIA2, IB3 greater than 6cm, IIB–IVA, or with lymph node involvement), or those at another stage who are not suitable for surgery
  • People with either no distant spread or some distant spread, where the treating team has approved a full course of local radiation treatment over 25 sessions

Bladder cancer group:

  • People approved for radiotherapy to the bladder (whole bladder or a targeted boost to the tumour area)
  • People with bladder cancer confirmed by a tissue sample
  • People whose cancer has been assessed within a certain stage range (cT1–4)
  • People where lymph nodes are either clear or have a limited level of involvement after initial treatment

Lung cancer group:

  • People approved for radiotherapy for lung cancer that has spread to nearby lymph nodes
  • People with non-small cell lung cancer, either confirmed by tissue sample or with strong enough clinical evidence to treat with radiotherapy
  • People whose cancer falls within certain tumour and lymph node stage ranges (cT1–4, cN1–3)
  • People with either no distant spread or some distant spread, where the treating team has approved a radical course of radiotherapy over 24 sessions

Head and neck cancer group:

  • People approved for radiotherapy for head and neck cancer
  • People with cancer of the throat, mouth, or voice box confirmed by a tissue sample
  • People whose cancer falls within certain tumour stage ranges (cT1–4) with any level of lymph node involvement, and where radiation to one or both sides of the neck is planned
  • People where no distant spread has been found

Who may not be able to join:

General (all groups):

  • People who are pregnant

Prostate cancer group:

  • People with a medical condition that significantly affects the quality of imaging scans used during treatment (for example, having a hip replacement)
  • People with severe urinary symptoms that the treating doctor believes could make the longer treatment sessions difficult to manage

Cervical cancer group:

  • People with a medical condition that significantly affects the quality of imaging scans used during treatment (for example, having a hip replacement)

Bladder cancer group:

  • People with a medical condition that significantly affects the quality of imaging scans used during treatment (for example, having a hip replacement)
  • People with severe urinary symptoms that the treating doctor believes could make the longer treatment sessions difficult to manage

Lung cancer group:

  • People with severe breathing difficulties that the treating doctor believes could make the longer treatment sessions difficult to manage

Head and neck cancer group:

  • People with severe symptoms that the treating doctor believes could make the longer treatment sessions difficult to manage
  • People with a lung condition called pulmonary fibrosis (scarring of the lungs)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +31205129140

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
The Netherlands Cancer Institute
Registry
ClinicalTrials.gov
Start date
29 August 2023
Est. completion
1 October 2028

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

Feasibility: successful application of the online adaptive treatment in 90% of 20 patients

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov