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Prostate-Rectal Separation With PEG Hydrogel and Its Effect on Decreasing Rectal Dose

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02212548
Recruitment Status : Completed
First Posted : August 8, 2014
Last Update Posted : June 14, 2021
Sponsor:
Information provided by (Responsible Party):
Professor Thomas Eade, Royal North Shore Hospital

Tracking Information
First Submitted Date  ICMJE June 5, 2012
First Posted Date  ICMJE August 8, 2014
Last Update Posted Date June 14, 2021
Actual Study Start Date  ICMJE March 2012
Actual Primary Completion Date December 2013   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: August 6, 2014)
  • % volume of rectum receiving 40Gy, 65Gy, 70Gy, 75Gy and 80Gy [ Time Frame: CT scans taken 1-2 weeks apart (Pre and post Hydrogel insertion) ]
    Estimated % volume of rectum as measured on CT dosimetry based on CT scans ore and post insertion of hydrogel taken 1-2 weeks apart (% volume of rectum receiving 40Gy, 65Gy, 70Gy, 75Gy and 80Gy).
  • Evaluation of serious adverse events or complications secondary to PEG hydrogel insertion. [ Time Frame: Post-Hydrogel Insertion then 2nd weekly during radiation therapy up to 9 weeks and at a 3 month follow-up. ]
    Physcian reported toxicity using CTC
Original Primary Outcome Measures  ICMJE Same as current
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: August 6, 2014)
Gastrointestinal toxicity [ Time Frame: Second weekly evaluation during radiation therapy up to 9 weeks and at 3 mths, 9 mths, 15 mths, 21 mths, 27mths and 36mths post treatment. ]
Patients will be physician scored using the CTC and patient scored using the EPIC QOL questionaire
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Prostate-Rectal Separation With PEG Hydrogel and Its Effect on Decreasing Rectal Dose
Official Title  ICMJE Prostate-Rectal Separation With PEG Hydrogel and Its Effect on Decreasing Rectal Dose
Brief Summary This is a Phase I prospective study of 30 patients to determine whether PEG hydrogel (SpaceOAR) reduces the dose of radiation delivered to the rectum during Image Guided Intensity Modulated Radiotherapy (IG-IMRT) for prostate cancer, by increasing the space between the prostate and the rectum.
Detailed Description

Patients who are referred to the Northern Sydney Cancer Centre for radiotherapy for treatment of their prostate cancer will be screened at the initial consultation for suitability for participation in the study. Following informed consent, those who agree to participate in the study will undergo the following procedures. Blood tests will be performed to ensure normal coagulation profile and renal function prior to any procedure. Under transrectal ultrasound guidance, patients will have insertion of fiducial gold seeds into the prostate under anaesthesia. While the patient is in theatre and under anaesthesia, the PEG hydrogel (SpaceOAR) will be inserted by Dr Thomas Eade, who will be competent in the procedure. The patient will be in the dorsal lithotomy position and prepared and draped. A transrectal ultrasound (TRUS) will be used for alignment of the needle and to ensure safe delivery. The hydrogel precursor and accelerator solutions will be mixed and connected to the Y connector that has been flushed with saline and to a syringe holder that ensures both syringe barrels are injected at the same time (comes with commercial product). The solutions will be injected within 30 minutes of mixing. After aspirating to ensure the tip of the needle is not intravascular, the perirectal space will be adequately dissected from the apex to midgland by injecting saline into the space between denonvilliers fascia and the anterior rectal space under TRUS guidance. This hydrodissection, prior to delivery of the hydrogel, should create a distance of 3-4 mm between the prostate and the rectum. Maintaining the needle position and angulation, the saline syringe is disconnected and the hydrogel system connected. After aspirating to ensure the needle tip is not in a blood vessel and under TRUS guidance, the hydrogel is injected in a smooth, continuous technique. The gel sets up within approximately 8 seconds.

In order to compare the effect of the PEG hydrogel (SpaceOAR) on the dose of radiation received by the rectum, two radiotherapy plans will be created. One planning CT scan will therefore be performed prior to the injection of the PEG hydrogel and one one week following injection of the hydrogel. The two treatment plans will be created by the same radiation therapist.

As the hydrogel is clearly visible on MRI and not on CT scans, we will obtain a pelvic MRI scan following injection of the hydrogel.. The MRI scans will be used in planning and fused to the planning CT scans to aid voluming.

Treatment:

Patients will undergo standard prostate cancer planning and treatment using image guided dose escalated IMRT as per the RNSH Department protocol and guidelines to a dose of 80Gy in 40 fractions 14.

Rectal Dose Analysis:

Two plans with dose-volume histograms will be created, one using the planning CT scan from prior to the PEG hydrogel (SpaceOAR) injection and one using the planning CT and MRI performed one week post hydrogel injection. MRI scans will be obtained on the same day as the CT simulation using the same bladder filling and rectal emptying protocols. Each patient will have two plans created by the same Radiation Therapist. This will allow for comparison between the 2 plans. The patient will be treated according to the post PEG hydrogel injection plan, with the initial plan for comparison purposes only. The volume of rectum receiving 80Gy, 75Gy, 70Gy, 65Gy, 60Gy, 40Gy, 35Gy and 25Gy will be compared with the two plans.

Patient assessment:

Patients will be assessed immediately post injection of the hydrogel, 24hrs later by telephone and 1 week later by telephone to determine if there has been any adverse event related to the PEG hydrogel (SpaceOAR) injection. This will include questions regarding pain or discomfort, infection, bleeding, and changes in bowel or bladder function. Information about every adverse event will be collected and recorded on the appropriate case report form. Adverse events will be described by duration (start and end dates), severity grade, and action taken. A follow-up report will follow the initial report within 5 working days. Any reports where the adverse event has not resolved at this time will be followed up to resolution of the event or until it becomes chronic and a statement is made to this effect.

During radiotherapy treatment patients will be assessed weekly in the clinic and their toxicity will be recorded using the modified RTOG and National Cancer Institute Common Terminology Criteria (v4.0) for adverse events.

Patients will be reviewed in the clinic 3 months, 9 months, 15 months and 21 months post completion of treatment and rectal toxicity will be assessed using the modified RTOG and National Cancer Institute Common Terminology Criteria (v4.0) for adverse events.

Adverse events:

An adverse event is any undesirable experience associated with the use of a medical product in a patient. All adverse events will be appropriately reported by duration (start and end dates), severity grade, and action taken on the appropriate case report form.

Grade 1 or mild events are easily tolerated. Grade 2 or moderate events cause enough discomfort to interfere with usual activity.

Grade 3 or severe events result in inability to carry out usual activities. Grade 4 events are life threatening or disabling. The serious adverse event will be documented and medically assessed by the investigator. As the PEG hydrogel cannot be removed following injection, patients will be treated medically and symptomatically. A follow-up report will follow the initial report within 5 working days. Any reports where the adverse event has not resolved at this time will be followed up to resolution of the event or until it becomes chronic and a statement is made to this effect.

Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Cancer of the Prostate
Intervention  ICMJE Device: PEG Hydrogel (SpaceOAR)
A single injection of PEG hydrogel (SpaceOAR) through the perineum under transrectal ultrasound guidance while under general anaesthetic.
Study Arms  ICMJE Experimental: Hydrogel
The patient will be in the dorsal lithotomy position and prepared and draped. A transrectal ultrasound (TRUS) will be used for alignment of the needle and to ensure safe delivery. The hydrogel precursor and accelerator solutions will be mixed and connected to the Y connector that has been flushed with saline and to a syringe holder that ensures both syringe barrels are injected at the same time. After aspirating to ensure the tip of the needle is not intravascular, the perirectal space will be adequately dissected from the apex to midgland by injecting saline into the space between denonvilliers fascia and the anterior rectal space under TRUS guidance. Maintaining the needle position and angulation, the saline syringe is disconnected and the hydrogel system connected. After aspirating to ensure the needle tip is not in a blood vessel and under TRUS guidance, the 'PEG Hydrogel (SpaceOAR) is injected in a smooth, continuous technique.
Intervention: Device: PEG Hydrogel (SpaceOAR)
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: August 6, 2014)
30
Original Estimated Enrollment  ICMJE Same as current
Actual Study Completion Date  ICMJE December 2016
Actual Primary Completion Date December 2013   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  1. Prostate cancer, confirmed with histopathology specimen;
  2. Eligible for prostate radiotherapy, either for definitive treatment or to aid local control in patients with known metastatic disease.

Exclusion criteria:

  1. Metastatic disease where local radiotherapy is not recommended management
  2. Complications following prostate biopsy including infection
  3. Urinary retention symptoms
  4. Bleeding disorder
  5. Renal impairment
  6. Anal fistula or perianal abscess
Sex/Gender  ICMJE
Sexes Eligible for Study: Male
Ages  ICMJE Child, Adult, Older Adult
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Australia
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT02212548
Other Study ID Numbers  ICMJE Hydrogel
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE
Plan to Share IPD: Yes
Plan Description: Other centres with ethics approval to use annonymised data
Responsible Party Professor Thomas Eade, Royal North Shore Hospital
Study Sponsor  ICMJE Royal North Shore Hospital
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Thomas Eade, MD Royal North Shore Hospital
PRS Account Royal North Shore Hospital
Verification Date June 2021

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP