Your session is about to expire
← Back to Search
Device
Blue Halo Coil Catheter for Urinary Retention (BlueHaloCoil Trial)
N/A
Recruiting
Research Sponsored by Blue Halo Biomedical, LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 56 days
Awards & highlights
No Placebo-Only Group
Summary
This trial studies a special tube called the Blue Halo Coil Catheter, designed to help men with an enlarged prostate who have trouble urinating. The device helps drain the bladder more effectively and is used temporarily for a few weeks.
Who is the study for?
Men over 50 with urinary retention due to BPH, who have a post void residual >350cc and prostate volume >50cc or urethral length of 5+ cm. They must be able to consent and attend appointments. Excluded are those with urethral strictures, gross hematuria, cognitive impairments, history of prostate cancer, high PSA density (>0.1), or on certain prostate medications.
What is being tested?
The trial is testing the 'Blue Halo Coil Catheter' in men who can't empty their bladders fully because of an enlarged prostate (BPH). The goal is for participants to resume normal urination with less than 75 cc left after voiding.
What are the potential side effects?
Potential side effects may include discomfort during catheter use, urinary tract infections from repeated catheterization, possible injury to the urethra or bladder, and irritation leading to increased urgency or frequency of urination.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 56 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~56 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
The change in Post Void Residual from baseline to day 28 will be measured and reported
Secondary study objectives
Primary safety endpoint adverse event and device removal
Secondary Safety Endpoint 1, incidence of device encrustation at removal
Secondary Safety Endpoint 2,urinary obstruction due to device migration
+1 moreOther study objectives
Bacterial Infection Monitoring
Quality of Life Measurement, no scale to report
Trends in Renal Function
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Blue Halo Coil Catheter for Urinary RetentionExperimental Treatment1 Intervention
The indication for use of the Blue Halo Coil Catheter is to facilitate bladder drainage in adult male patients with urinary retention due to benign prostatic hyperplasia. The device is inserted for temporary use up to 28 days.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for urinary retention include catheterization, alpha-1-adrenergic antagonists, and surgical interventions. Catheterization, either intermittent or indwelling, mechanically drains the bladder, providing immediate relief from retention.
Alpha-1-adrenergic antagonists, such as tamsulosin, work by relaxing the smooth muscle in the bladder neck and prostate, reducing resistance to urine flow and facilitating voiding. Surgical interventions, like transurethral resection of the prostate (TURP), remove or reduce prostate tissue obstructing the urethra, significantly lowering the risk of acute urinary retention.
These treatments are crucial as they address the underlying causes of retention, improve bladder emptying, and reduce complications associated with high PVR, enhancing the quality of life for patients.
Urodynamics of the female lower urinary tract.The role of perioperative medications in urinary retention following midurethral sling.Repeat post-op voiding trials: an inconvenient correlate with success.
Urodynamics of the female lower urinary tract.The role of perioperative medications in urinary retention following midurethral sling.Repeat post-op voiding trials: an inconvenient correlate with success.
Find a Location
Who is running the clinical trial?
Blue Halo Biomedical, LLCLead Sponsor
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have trouble fully emptying my bladder, leaving more than 350 cc.I have visible blood in my urine.I am a man over 50 years old.I am able to understand and agree to the study's requirements.I have a history of prostate cancer.My urinary issues are due to an enlarged prostate.I am currently taking hormone therapy for cancer.I am currently taking alpha-blockers or 5-alpha-reductase inhibitors.I will undergo a biopsy for my prostate nodule to check for cancer.I have a PSA over 4 and density over 0.1, and will undergo a biopsy to check for prostate cancer.
Research Study Groups:
This trial has the following groups:- Group 1: Blue Halo Coil Catheter for Urinary Retention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger