Localized Prostate CancerPRECISIONNCT06117059
The PRECISION Study: 3 Fractions of Prostate SBRT and RayPilot HypoCath Image Guidance
A study testing 3 fractions of prostate SBRT in people with Localized Prostate Cancer and Low Risk Prostate Cancer, run by NHS Lothian at 1 site in United Kingdom.
Trial summary
The investigators want to investigate whether it is possible to reduce the number of curative radiotherapy doses from 5 to only 3 for men with localized early prostate cancer. The aim of the study is to ensure that the side effects of the 3-dose treatment are the same or potentially lower than those already published… Read more about this study
- Who is it for?
- Any age, men only
- Conditions the study is for
- Localized Prostate Cancer, Low Risk Prostate Cancer, Intermediate Risk Prostate Cancer
- What is being tested?
- 3 fractions of prostate SBRT
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 1 Nov 2024to 1 Nov 2027
- 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 Any age
- Men only
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- low and favorable intermediate NCCN Criteria patients
- Prostate volume under 80cc
- IPSS under 20
- Q-max above 10cc per second and urinary residual less than 150mls
- No TURP
- No hip replacements
Show all 11Show fewer
- No previous radiotherapy to the pelvis
- No active second malignancy except skin SCC or BCC for the last 2 years
- No history of inflammatory bowel disease
- No co-morbid illness that would make compliance to treatment difficult
- Able to give informed consent
Who cannot join
- T3a or above
- Gleason 4+3=7
- PSA>20ng/ml
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United Kingdom1 site, 1 recruiting
- Recruiting
NHS Lothian
Edinburgh
Duncan Mclaren
About this study
Official title: The PRECISION Study: A Phase II Study of 3 Fractions of Prostate SBRT With RayPilot System and HypoCath Image Guidance for Men With NCCN Low or Intermediate Risk Prostate Cancer
The investigators want to investigate whether it is possible to reduce the number of curative radiotherapy doses from 5 to only 3 for men with localized early prostate cancer. The aim of the study is to ensure that the side effects of the 3-dose treatment are the same or potentially lower than those already published when using the 5-dose treatment as used in the UK PACE-B trial (NCT01584258). The name of this type of radiotherapy is Stereotactic Body Radiotherapy (SBRT) or participants may see it referred to as Stereotactic Ablative Radiotherapy (SABR). The study is a two-stage single arm Phase II study open to those Centres that use the RayPilot HypoCath tumour tracking system (Micropos Medical). This commercially available system was not available at the time of the original PACE-B study. The system acts like a Global Positioning Device (GPS) to continuously track the prostate position during radiotherapy. If the prostate moves more than 2mm (about 0.08 in) from its intended position during the treatment, then the radiotherapy team are alerted, and the treatment halted until the prostate moves back into the correct position. The ability to understand exactly where the prostate is throughout the treatment ensures the intended dose hits the cancer and does not accidentally increase the dose to the nearby bladder and rectum. The system is a modification of a standard urinary catheter which sits within the bladder with the GPS placed within the wall of the catheter as it passes through the prostate. The investigators are not testing the system as it is commercially available but using it to improve the accuracy of radiotherapy delivery, reducing the number of days of treatment, minimizing side effects and helping ease the burden on busy radiotherapy Departments.
Read the detailed description
Prostate cancer is the commonest male cancer and sadly more than 10,000 men die each year from the disease in the UK. This is actually a greater number than women who die from breast cancer each year in the UK. If diagnosed at an early stage, the chances of being cured of the disease are high through either surgery (prostatectomy) to remove the prostate or through radiation treatment (radiotherapy). Both treatment options are associated with quality of life changing impacts on sexual, bowel and bladder function, with survivors having to manage these side effects for the rest of their lives. It is a key area of research to try and identify who may be at particular risk and to minimize these risks. The development of increasingly sophisticated radiotherapy machines (linear accelerators) which can deliver radiotherapy more precisely has allowed the radiotherapy for prostate cancer to be transformed over the last decade. The number of treatments required for cure has been reduced from 39 over nearly 8 weeks, to 20 over 4 weeks, and more recently to only 5 over 1-2 weeks, greatly improving patient convenience through less travel, days off work, or time in hospital away from loved ones. Importantly technology has reduced but not removed the risk of both initial and then longer term permanent side effects.
In this study the investigators want to reduce the number of treatments down to only 3, given on consecutive days, further enhancing the patient experience and providing evidence that this number of treatments could become the new standard of care. In this study the investigators will be using the very latest state of the art radiotherapy machines and the unique RayPilot system, adopted for routine use by a small number of global radiotherapy centres when delivering prostate SBRT(Stereotactic Body Radiotherapy). The ability to track the position of the prostate cancer throughout the radiotherapy treatment using RayPilot allows the treatment to be given more precisely with less dose being given to the surrounding bladder and rectum. It also ensures that all the intended dose is given to the cancer as the treatment can be interrupted should the cancer move due to rectal gas, changes in bladder filling or simply the patient moving position on the treatment bed, maximizing the chances of cure and minimizing the risk of life changing side effects.
This is a single arm 2 stage Phase II study that will test the safety of the 3 fraction radiotherapy schedule. It has built in safety measures to ensure that the immediate post treatment side effects on the bowel and bladder are within the expected limits of acceptance at 12 weeks post completion of treatment. After 43 patients are recruited the initial data will be analyzed and if acceptable the study will continue until all 100 patients have been recruited. The study will be opened in the UK with Edinburgh as the lead Centre, and also in a number of other global centres each of which will ask for their own local ethical approval and sponsorship. The anonymized data from each Centre will be recorded on a trial specific RedCap database held by the University of Edinburgh for analysis of the trial results.
On the day of treatment planning, the patient will be met by the research team and taken to the MRI suite. Patients will have already have been prescribed a rectal suppository by their GP to bring with them. The patient will be directed to the toilet at the MRI scanner and will pass the suppository into their rectum and wait 30 seconds before evacuating it. The aim is to dispel rectal gas not necessarily to move the bowels. Patients will also empty their bladder of urine. The research nurse or radiographer will then place a dummy RayPilot HypoCath (called a ViewCath) or a simple standard Foley urinary catheter if preferred, and fill the bladder with 100-150 mls of water. This volume is recorded and kept as a constant for each day of subsequent treatment. An MRI of the prostate is then performed with standard T1 and T2 anatomical images and functional Dynamic Contrast Enhanced (DCE) and diffusion weighted (DW) sequences that identify the tumour. The MRI scan will last approximately 20minutes. On completion the patient is then taken for the planning CT scan within the Radiotherapy Department. The bladder is drained and then refilled through the catheter to the same volume as the MRI scan. The suppository is only repeated if there has been a substantial change in the rectal volume between the MRI and planning CT scan. The CT scan takes 15 minutes and then the patient has the catheter removed and is free to go home.
The MRI and CT scan are fused together to allow the clinician to plan the radiotherapy treatment on the radiotherapy planning computer system. Once the target and surrounding normal tissues have been outlined and a radiotherapy plan developed then the patient is ready to start treatment. The planning of treatment takes 2 weeks on average.
On the day of treatment the patient will be met in the Radiotherapy Department by the research team and taken to the treatment machine. A baseline PSA (Prostate Specific Antigen) should have been taken prior to the start date however if not then this blood test will be performed by the research team. A baseline quality of life patient reported outcome measure (PROM) consisting of IPSS (International Prostate Symptom Score), EPIC-26 (Expanded Prostate Cancer Index Composite), EIIF-5 (International Index of Erectile Function), Vaizey Score (A measure of bowel symptoms including incontinence)and clinician assessed RTOG (Radiotherapy and Oncology Group)and CTCAE (Common Terminology Criteria for Adverse Events) bowel and bladder toxicity scores taken. These forms will take approximately 20 minutes to complete.
The patient will then use a rectal suppository in the toilet as per the planning scans and empty their bladder. The research team will then place the RayPilot HypoCath into the bladder under local anesthetic. This procedure is no different to placing a normal Foley urinary catheter. The bladder will be filled with the same volume of water used at the time of the planning scans and is then ready for treatment.
Patients lie on their back in the linear accelerator on a special RayPilot receiver couch top with their ankles resting on foot stocks to reduce movement. The patient is set up for treatment as per standard of care when delivering prostate SBRT. A check cone beam CT scan taken by the linear accelerator is taken to verify the treatment position and that the prostate is correctly within the radiotherapy field. If this is correct the treatment beam is switched on and treatment starts. Should the prostate move beyond the 2mm level of tolerance set for the treatment then the beam is interrupted and restarted when the prostate has returned to the correct position. If needed a repeat cone beam treatment CT may be taken before the beam is switched on should the prostate fail to settle back into position and the patients new treatment position used. The time taken to deliver the treatment from entering the linear accelerator to leaving the room is 20-30 minutes. On completion of the first day of treatment the patient drains the bladder and a flip flow valve placed on the end of the RayPilot HypoCath to allow the patient to continue to pass urine as needed by simply opening the valve and letting the bladder drain through the catheter into the toilet.
The patient will start their treatment on a Tuesday if possible and be treated on 3 consecutive days in total. On day 2 and 3 the treatment procedure is identical to the day 1. On completion of treatment on day 3 the HypoCath is removed and repeat RTOG and CTCAE toxicity and an IPSS assessment taken by the research team before the patient goes home.
The patients are then followed up in the outpatient clinical by the research team and the follow up PSA and toxicity assessments are made. The follow up schedule is weeks, 2, 4, 8 and 12 post treatment, and then months 6, 9, 12, 18 and 24 before they then leave the study. Prior to each visit the local GP/ Community practice will have taken the PSA blood test to assess tumour response. If this has not been done prior to clinic then it will be taken by the research team in the clinic. PSA blood tests at FU are standard procedure and the interval is the same as men treated by prostate SBRT who are not in the study except for an extra visit at weeks 2 and month 9 for this study.
The level of acute radiotherapy side effects up to and including week 12 will be assessed as follows RTOG/CTCAE \& IPSS weeks 2, 4, 8, 12 EPIC-26 \& Vaizey Score weeks 4 and 12 IIEF-5 week 12. The anticipated length of each clinic visit will be 20 minutes The level of late persistent radiotherapy side effects up to and including month 24 be asses as follows RTOG/CTCAE, IPSS, EPIC-26 \& VAIZEY Score at months 6,9, 12, 18, 24 IIEF-5 at months 6, 12 and 24 only. After 24 months patients will leave the study and be followed up within the Departmental follow up policy for long term outcome data
- Being tested
- 3 fractions of prostate SBRT
- Keywords
- SBRT, SABR, PROSTATE CANCER, RayPilot, HypoCath, Continuous tracking, 3 fractions
- Medical subject headings
- Prostatic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
3 fractions of prostate SBRTRadiation
Radical radiotherapy using only 3 fractions of prostate SBRT over 3 consecutive days
| Study group | Role | What they receive |
|---|---|---|
| 3 fractions of prostate Stereotactic Body Radiotherapy (SBRT) | Experimental | 3 fractions of SBRT with image guidance using the RayPilot HypoCath system given on 3 consecutive days Receives: Radiation: 3 fractions of prostate SBRT |
What is being measured
The primary outcome is the main question the study is designed to answer.
The number of patients with acute Radiation Oncology/ Toxicity Grading (RTOG) urinary toxicity
Clinician reported cumulative Grade 2 or worse RTOG acute GU toxicity from baseline up to 12 weeks post treatment (scale 0-4 with 0 being none increasing severity to grade 4).
Measured: At 12 weeks post completion of treatment
The number of patients with acute Common Terminology for Adverse Events (CTCAE) urinary toxicity
Clinician reported cumulative Grade 2 or worse CTCAE v5.0 acute GU toxicity from baseline up to 12 weeks post treatment (scale 0-5 with increasing severity to death at grade 5)
Measured: At 12 weeks post completion of treatment
The number of patients with acute Radiation Oncology/ Toxicity Grading (RTOG) bowel toxicity
Clinician reported cumulative Grade 2 or worse RTOG acute GI toxicity from baseline up to 12 weeks post treatment (scale 0-4 with 0 being none increasing severity to grade 4).
Measured: At 12 weeks post treatment
The number of patients with acute Common Terminology for Adverse Events (CTCAE) bowel toxicity
Clinician reported cumulative Grade 2 or worse CTCAE v5.0 acute GI toxicity from baseline up to 12 weeks post treatment (scale 0-5 with increasing severity to death at grade 5).
Measured: At 12 weeks
Secondary outcomes (12)
The number of patients with late Radiation Oncology/ Toxicity Grading (RTOG) urinary toxicity
Clinician reported Grade 2 or worse RTOG late GU toxicity at 24 months (scale 0-4 with 0 being none increasing severity to grade 4).
Measured: At 24 months post completion of radiotherapy treatment
The number of patients with late Common Terminology for Adverse Events (CTCAE) urinary toxicity
Clinician reported Grade 2 or worse CTCAE v5.0 late GU toxicity at 24 months (scale 0-5 with increasing severity to death at grade 5).
Measured: At 24 months post completion of radiotherapy treatment
The number of patients with late Radiation Oncology/ Toxicity Grading (RTOG) bowel toxicity
Clinician reported Grade 2 or worse RTOG late GI toxicity at 24 months (scale 0-4 with 0 being none increasing severity to grade 4).
Measured: At 24 months post completion of radiotherapy treatment
The number of patients with late Common Terminology for Adverse Events (CTCAE) bowel toxicity
Clinician reported Grade 2 or worse CTCAE v5.0 late GI toxicity at 24 months (scale 0-5 with increasing severity to death at grade 5).
Measured: At 24 months post completion of radiotherapy treatment
Cumulative number of patients who experienced late Radiation Oncology/ Toxicity Grading (RTOG) urinary toxicity
Clinician reported cumulative Grade 2 or worse RTOG late GU toxicity from 6 months to 24 months post treatment (scale 0-4 with 0 being none increasing severity to grade 4).
Measured: From 6-24 months
Cumulative number of patients who experience late Common Terminology for Adverse Events (CTCAE) urinary toxicity
Clinician reported cumulative Grade 2 or worse CTCAE v5.0 late GU toxicity from 6 months to 24 months post treatment (scale 0-5 with increasing severity to death at grade 5).
Measured: From 6-24 months
Cumulative number of patients who experience late Radiation Oncology/ Toxicity Grading (RTOG) bowel toxicity
Clinician reported cumulative Grade 2 or worse RTOG late GI toxicity from 6 months to 24 months post treatment (scale 0-4 with 0 being none increasing severity to grade 4).
Measured: From 6-24 months
Cumulative number of patients who experience late Common Terminology for Adverse Events (CTCAE) bowel toxicity
Clinician reported cumulative Grade 2 or worse CTCAEv5.0 late GI toxicity from 6 months to 24 months post treatment (scale 0-5 with increasing severity to death at grade 5).
Measured: From 6-24 months
Quality of life patient reported outcome measure Expanded Prostate Index Composite-26 (EPIC-26)
Expanded Prostate Index Composite-26 (EPIC-26), patient reported outcome measure of urinary, bowel, sexual, physical and mental health
Measured: Pre treatment to 24 months post treatment
Quality of life patient reported outcome measure International Prostate Symptom Score (IPSS)
International Prostate Symptom Score (IPSS), a patient reported outcome measure of urinary bother
Measured: Pre treatment to 24 months post treatment
Quality of life patient reported outcome measure International Index of Erectile Function-5 (IIEF-5)
International Index of Erectile Function-5 (IIEF-5), a patient reported outcome measure of erectile and sexual function
Measured: Pre treatment to 24 months post treatment
Quality of life patient reported outcome measure Vaizy Score
Vaizey score, a patient reported assessment of bowel function
Measured: Pre treatment to 24 months post treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Nov 2023
- Study start1 Nov 2024
- Primary completion1 Nov 2026 (estimated)
- Study completion1 Nov 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Localized Prostate 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
- Not applicable
- Intervention model
- Single group
- Model description
- Single arm Phase II study of 3 fractions of prostate SBRT
- Masking
- None (open label)
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- NHS Lothian
- Sponsor type
- Other government
- Responsible party
- Sponsor
- Investigators
- Duncan B McLaren, MBBS, Principal investigator, NHS Lothian & University of Edinburgh
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06117059
- Sponsor's protocol ID
- AC23118
- Acronym
- PRECISION
- Status last verified
- Jan 2026
- First submitted
- 10 Oct 2023
- Last updated
- 12 Jan 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: The data generated is specific to using the RayPilot HypoCath System when delivering the treatment. Results will be presented and published but individual patient data would not be supplied
Study at a glance
From the registry record, last updated by the sponsor on 12 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The PRECISION Study: A Phase II Study of 3 Fractions of Prostate SBRT With RayPilot System and HypoCath Image Guidance for Men With NCCN Low or Intermediate Risk Prostate Cancer
- ClinicalTrials.gov ID
- NCT06117059
- Acronym / sponsor ID
- PRECISION / AC23118
- Keywords
- SBRT, SABR, PROSTATE CANCER, RayPilot, HypoCath, Continuous tracking, 3 fractions
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- NHS LothianOther government
- Study start
- 1 Nov 2024 (actual)
- Primary completion
- 1 Nov 2026 (estimated)
- Study completion
- 1 Nov 2027 (estimated)
- First posted
- 3 Nov 2023 (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 investigators want to investigate whether it is possible to reduce the number of curative radiotherapy doses from 5 to only 3 for men with localized early prostate cancer. The aim of the study is to ensure that the side effects of the 3-dose treatment are the same or potentially lower than those already published when using the 5-dose treatment as used in the UK PACE-B trial (NCT01584258). The name of this type of radiotherapy is Stereotactic Body Radiotherapy (SBRT) or participants may see it referred to as Stereotactic Ablative Radiotherapy (SABR). The study is a two-stage single arm Phase II study open to those Centres that use the RayPilot HypoCath tumour tracking system (Micropos Medical). This commercially available system was not available at the time of the original PACE-B study. The system acts like a Global Positioning Device (GPS) to continuously track the prostate position during radiotherapy. If the prostate moves more than 2mm (about 0.08 in) from its intended position during the treatment, then the radiotherapy team are alerted, and the treatment halted until the prostate moves back into the correct position. The ability to understand exactly where the prostate is throughout the treatment ensures the intended dose hits the cancer and does not accidentally increase the dose to the nearby bladder and rectum. The system is a modification of a standard urinary catheter which sits within the bladder with the GPS placed within the wall of the catheter as it passes through the prostate. The investigators are not testing the system as it is commercially available but using it to improve the accuracy of radiotherapy delivery, reducing the number of days of treatment, minimizing side effects and helping ease the burden on busy radiotherapy Departments.
Detailed description
Prostate cancer is the commonest male cancer and sadly more than 10,000 men die each year from the disease in the UK. This is actually a greater number than women who die from breast cancer each year in the UK. If diagnosed at an early stage, the chances of being cured of the disease are high through either surgery (prostatectomy) to remove the prostate or through radiation treatment (radiotherapy). Both treatment options are associated with quality of life changing impacts on sexual, bowel and bladder function, with survivors having to manage these side effects for the rest of their lives. It is a key area of research to try and identify who may be at particular risk and to minimize these risks. The development of increasingly sophisticated radiotherapy machines (linear accelerators) which can deliver radiotherapy more precisely has allowed the radiotherapy for prostate cancer to be transformed over the last decade. The number of treatments required for cure has been reduced from 39 over nearly 8 weeks, to 20 over 4 weeks, and more recently to only 5 over 1-2 weeks, greatly improving patient convenience through less travel, days off work, or time in hospital away from loved ones. Importantly technology has reduced but not removed the risk of both initial and then longer term permanent side effects.
In this study the investigators want to reduce the number of treatments down to only 3, given on consecutive days, further enhancing the patient experience and providing evidence that this number of treatments could become the new standard of care. In this study the investigators will be using the very latest state of the art radiotherapy machines and the unique RayPilot system, adopted for routine use by a small number of global radiotherapy centres when delivering prostate SBRT(Stereotactic Body Radiotherapy). The ability to track the position of the prostate cancer throughout the radiotherapy treatment using RayPilot allows the treatment to be given more precisely with less dose being given to the surrounding bladder and rectum. It also ensures that all the intended dose is given to the cancer as the treatment can be interrupted should the cancer move due to rectal gas, changes in bladder filling or simply the patient moving position on the treatment bed, maximizing the chances of cure and minimizing the risk of life changing side effects.
This is a single arm 2 stage Phase II study that will test the safety of the 3 fraction radiotherapy schedule. It has built in safety measures to ensure that the immediate post treatment side effects on the bowel and bladder are within the expected limits of acceptance at 12 weeks post completion of treatment. After 43 patients are recruited the initial data will be analyzed and if acceptable the study will continue until all 100 patients have been recruited. The study will be opened in the UK with Edinburgh as the lead Centre, and also in a number of other global centres each of which will ask for their own local ethical approval and sponsorship. The anonymized data from each Centre will be recorded on a trial specific RedCap database held by the University of Edinburgh for analysis of the trial results.
On the day of treatment planning, the patient will be met by the research team and taken to the MRI suite. Patients will have already have been prescribed a rectal suppository by their GP to bring with them. The patient will be directed to the toilet at the MRI scanner and will pass the suppository into their rectum and wait 30 seconds before evacuating it. The aim is to dispel rectal gas not necessarily to move the bowels. Patients will also empty their bladder of urine. The research nurse or radiographer will then place a dummy RayPilot HypoCath (called a ViewCath) or a simple standard Foley urinary catheter if preferred, and fill the bladder with 100-150 mls of water. This volume is recorded and kept as a constant for each day of subsequent treatment. An MRI of the prostate is then performed with standard T1 and T2 anatomical images and functional Dynamic Contrast Enhanced (DCE) and diffusion weighted (DW) sequences that identify the tumour. The MRI scan will last approximately 20minutes. On completion the patient is then taken for the planning CT scan within the Radiotherapy Department. The bladder is drained and then refilled through the catheter to the same volume as the MRI scan. The suppository is only repeated if there has been a substantial change in the rectal volume between the MRI and planning CT scan. The CT scan takes 15 minutes and then the patient has the catheter removed and is free to go home.
The MRI and CT scan are fused together to allow the clinician to plan the radiotherapy treatment on the radiotherapy planning computer system. Once the target and surrounding normal tissues have been outlined and a radiotherapy plan developed then the patient is ready to start treatment. The planning of treatment takes 2 weeks on average.
On the day of treatment the patient will be met in the Radiotherapy Department by the research team and taken to the treatment machine. A baseline PSA (Prostate Specific Antigen) should have been taken prior to the start date however if not then this blood test will be performed by the research team. A baseline quality of life patient reported outcome measure (PROM) consisting of IPSS (International Prostate Symptom Score), EPIC-26 (Expanded Prostate Cancer Index Composite), EIIF-5 (International Index of Erectile Function), Vaizey Score (A measure of bowel symptoms including incontinence)and clinician assessed RTOG (Radiotherapy and Oncology Group)and CTCAE (Common Terminology Criteria for Adverse Events) bowel and bladder toxicity scores taken. These forms will take approximately 20 minutes to complete.
The patient will then use a rectal suppository in the toilet as per the planning scans and empty their bladder. The research team will then place the RayPilot HypoCath into the bladder under local anesthetic. This procedure is no different to placing a normal Foley urinary catheter. The bladder will be filled with the same volume of water used at the time of the planning scans and is then ready for treatment.
Patients lie on their back in the linear accelerator on a special RayPilot receiver couch top with their ankles resting on foot stocks to reduce movement. The patient is set up for treatment as per standard of care when delivering prostate SBRT. A check cone beam CT scan taken by the linear accelerator is taken to verify the treatment position and that the prostate is correctly within the radiotherapy field. If this is correct the treatment beam is switched on and treatment starts. Should the prostate move beyond the 2mm level of tolerance set for the treatment then the beam is interrupted and restarted when the prostate has returned to the correct position. If needed a repeat cone beam treatment CT may be taken before the beam is switched on should the prostate fail to settle back into position and the patients new treatment position used. The time taken to deliver the treatment from entering the linear accelerator to leaving the room is 20-30 minutes. On completion of the first day of treatment the patient drains the bladder and a flip flow valve placed on the end of the RayPilot HypoCath to allow the patient to continue to pass urine as needed by simply opening the valve and letting the bladder drain through the catheter into the toilet.
The patient will start their treatment on a Tuesday if possible and be treated on 3 consecutive days in total. On day 2 and 3 the treatment procedure is identical to the day 1. On completion of treatment on day 3 the HypoCath is removed and repeat RTOG and CTCAE toxicity and an IPSS assessment taken by the research team before the patient goes home.
The patients are then followed up in the outpatient clinical by the research team and the follow up PSA and toxicity assessments are made. The follow up schedule is weeks, 2, 4, 8 and 12 post treatment, and then months 6, 9, 12, 18 and 24 before they then leave the study. Prior to each visit the local GP/ Community practice will have taken the PSA blood test to assess tumour response. If this has not been done prior to clinic then it will be taken by the research team in the clinic. PSA blood tests at FU are standard procedure and the interval is the same as men treated by prostate SBRT who are not in the study except for an extra visit at weeks 2 and month 9 for this study.
The level of acute radiotherapy side effects up to and including week 12 will be assessed as follows RTOG/CTCAE \& IPSS weeks 2, 4, 8, 12 EPIC-26 \& Vaizey Score weeks 4 and 12 IIEF-5 week 12. The anticipated length of each clinic visit will be 20 minutes The level of late persistent radiotherapy side effects up to and including month 24 be asses as follows RTOG/CTCAE, IPSS, EPIC-26 \& VAIZEY Score at months 6,9, 12, 18, 24 IIEF-5 at months 6, 12 and 24 only. After 24 months patients will leave the study and be followed up within the Departmental follow up policy for long term outcome data
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Single arm Phase II study of 3 fractions of prostate SBRT
| Arm | Type | Receives |
|---|---|---|
| 3 fractions of prostate Stereotactic Body Radiotherapy (SBRT) | Experimental | Radiation: 3 fractions of prostate SBRT3 fractions of SBRT with image guidance using the RayPilot HypoCath system given on 3 consecutive days |
Who may qualify
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (11 listed)
- low and favorable intermediate NCCN Criteria patients
- Prostate volume under 80cc
- IPSS under 20
- Q-max above 10cc per second and urinary residual less than 150mls
- No TURP
Key exclusion criteria (3 listed)
- T3a or above
- Gleason 4+3=7
- PSA>20ng/ml
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 |
|---|---|---|
| 3 fractions of prostate SBRTRadical radiotherapy using only 3 fractions of prostate SBRT over 3 consecutive days | Radiation | 3 fractions of prostate Stereotactic Body Radiotherapy (SBRT) |
Primary outcome
The number of patients with acute Radiation Oncology/ Toxicity Grading (RTOG) urinary toxicity
Time frame: At 12 weeks post completion of treatment
Clinician reported cumulative Grade 2 or worse RTOG acute GU toxicity from baseline up to 12 weeks post treatment (scale 0-4 with 0 being none increasing severity to grade 4).
The number of patients with acute Common Terminology for Adverse Events (CTCAE) urinary toxicity
Time frame: At 12 weeks post completion of treatment
Clinician reported cumulative Grade 2 or worse CTCAE v5.0 acute GU toxicity from baseline up to 12 weeks post treatment (scale 0-5 with increasing severity to death at grade 5)
The number of patients with acute Radiation Oncology/ Toxicity Grading (RTOG) bowel toxicity
Time frame: At 12 weeks post treatment
Clinician reported cumulative Grade 2 or worse RTOG acute GI toxicity from baseline up to 12 weeks post treatment (scale 0-4 with 0 being none increasing severity to grade 4).
The number of patients with acute Common Terminology for Adverse Events (CTCAE) bowel toxicity
Time frame: At 12 weeks
Clinician reported cumulative Grade 2 or worse CTCAE v5.0 acute GI toxicity from baseline up to 12 weeks post treatment (scale 0-5 with increasing severity to death at grade 5).
12 secondary outcomes
The number of patients with late Radiation Oncology/ Toxicity Grading (RTOG) urinary toxicity
Time frame: At 24 months post completion of radiotherapy treatment
The number of patients with late Common Terminology for Adverse Events (CTCAE) urinary toxicity
Time frame: At 24 months post completion of radiotherapy treatment
The number of patients with late Radiation Oncology/ Toxicity Grading (RTOG) bowel toxicity
Time frame: At 24 months post completion of radiotherapy treatment
The number of patients with late Common Terminology for Adverse Events (CTCAE) bowel toxicity
Time frame: At 24 months post completion of radiotherapy treatment
Cumulative number of patients who experienced late Radiation Oncology/ Toxicity Grading (RTOG) urinary toxicity
Time frame: From 6-24 months
Cumulative number of patients who experience late Common Terminology for Adverse Events (CTCAE) urinary toxicity
Time frame: From 6-24 months
Cumulative number of patients who experience late Radiation Oncology/ Toxicity Grading (RTOG) bowel toxicity
Time frame: From 6-24 months
Cumulative number of patients who experience late Common Terminology for Adverse Events (CTCAE) bowel toxicity
Time frame: From 6-24 months
Quality of life patient reported outcome measure Expanded Prostate Index Composite-26 (EPIC-26)
Time frame: Pre treatment to 24 months post treatment
Quality of life patient reported outcome measure International Prostate Symptom Score (IPSS)
Time frame: Pre treatment to 24 months post treatment
Quality of life patient reported outcome measure International Index of Erectile Function-5 (IIEF-5)
Time frame: Pre treatment to 24 months post treatment
Quality of life patient reported outcome measure Vaizy Score
Time frame: Pre treatment to 24 months post treatment
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 12 Jan 2026.
- Individual participant dataSharing planned: No. The data generated is specific to using the RayPilot HypoCath System when delivering the treatment. Results will be presented and published but individual patient data would not be supplied
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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.
Duncan B McLaren, MBBS principal investigator
NHS Lothian & University of Edinburgh
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing 3 fractions of prostate SBRT in people with Localized Prostate Cancer and Low Risk Prostate Cancer, run by NHS Lothian at 1 site in United Kingdom.
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 11 inclusion and 3 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 12 Jan 2026. 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 United Kingdom. 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 Richard Allan (+44 1315371463, richard.allan@nhslothian.scot.nhs.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The number of patients with acute Radiation Oncology/ Toxicity Grading (RTOG) urinary toxicity (time frame: At 12 weeks post completion of treatment). The study lists 4 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 12 Jan 2026.