Last reviewed · How we verify
NCT03843073
Connected Catheter- Safety and Effectiveness Study
NA trial testing Connected Urinary Catheter in Urinary Retention in 9 participants. Terminated before completion.
23 March 2021
Quick facts
| Lead sponsor | Spinal Singularity |
|---|---|
| Phase | NA |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 9 |
| Start date | 16 October 2020 |
| Primary completion | 23 March 2021 |
| Estimated completion | 6 April 2021 |
| Sites | 9 locations across United States |
Drugs / interventions tested
- Connected Urinary Catheter
Conditions studied
- Urinary Retention — all drugs for Urinary Retention →
- Neurogenic Bladder — all drugs for Neurogenic Bladder →
- Urologic Diseases — all drugs for Urologic Diseases →
Sponsor
Spinal Singularity
Who can join
18 and older, male only, with Urinary Retention or Neurogenic Bladder. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The Connected Catheter is a fully internal, urethral indwelling urinary prosthesis designed for improved bladder management in males with urinary retention disorders requiring catheterization. It is a sterile, extended-use device that resides fully internally to the male lower urinary tract for an intended use life of up to 7 days per catheter.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT03843073
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Urinary Retention
Currently open trials in the same condition.
- NCT07372547 — Effect of Voiding Position (Standing in the Shower vs. Sitting) on Post-Void Residual Urine Volume (PVR) After Removal o · NA · recruiting
- NCT07355803 — Define Final Selection Choice Criteria for a Coloplast Catheter Ensuring Highest Patient Satisfaction Via Surveys (EVA). · NA · recruiting
- NCT06978205 — Effect of Urethral Balloon Dilatation on Urinary Retention After Spinal Cord Injury · NA · recruiting
- NCT06163469 — Effect of Chlorhexidine Gluconate Bladder Instillations in Patients With Chronic Suprapubic Catheters on Unplanned Healt · NA · recruiting
- NCT06179654 — Preoperative Pelvic Floor Physical Therapy to Minimize Stress Urinary Incontinence After Holmium Laser Enucleation of th · NA · recruiting
Other Spinal Singularity trials
Trials by the same sponsor.
- NCT05330598 — Evaluation of the Safety and Clinical Performance of the Connected Catheter Study · NA · terminated
- NCT04059159 — Connected Catheter - Safety and Effectiveness Study · NA · terminated
- NCT03626324 — Connected Catheter (C2P) Study for Bladder Management · NA · completed
- NCT03405285 — Connected Catheter Clinical Feasibility Study( CFS) · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03843073 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Spinal Singularity
- Last refreshed: 23 November 2021
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03843073.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing