Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06571058 · ClinicalTrials.gov registry record · NA

B3 Buddy for Securing Urinary Drainage Bag to Patient While Walking

A NA study, sponsored by Ohio State University Comprehensive Cancer Center.

Completed
Registry status
NA
Development phase
41
Enrollment target

NCT06571058: Completed NA study, sponsored by Ohio State University Comprehensive Cancer Center.

NCT06571058 is a NA study that has completed, run by Ohio State University Comprehensive Cancer Center. The registered enrollment target is 41 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06571058, a NA study, has completed, sponsored by Ohio State University Comprehensive Cancer Center.

COMPLETED
Registry status
NA
Development phase
41 participants
Enrollment target

Study Summary

This clinical trial tests how well the Bag Below Bladder (B3) Buddy device works in securing urinary drainage bags while walking. Keeping a urinary drainage bag below the bladder is the standard of care to maintain urine flow and prevent urine from backing up into the bladder. Despite the use of modern urinary drainage bags for over 60 years, workarounds, including hooking the bag into pants pockets, are being used to secure the bags while walking. The B3 Buddy may help keep the urinary drainage bag at the proper level for drainage while walking.

Primary Outcome

The proportion of patients who find the device acceptable will be determined with the Acceptability of Implementation Measure tool. he AIM has 4 Likert items, ranging from 1 (for "completely disagree") to 5 (for "completely agree"). A higher number indicates greater acceptability. If a patient marked 3 or more items with at least a "4," the device was considered acceptable. The device will be considered acceptable if at least 70% of patient participants find the device acceptable, which will be

Interventions

  • OTHER Questionnaire Administration
  • OTHER Medical Device Usage and Evaluation
  • OTHER Educational Intervention
  • DEVICE Medical Device Usage and Evaluation
  • OTHER Assistance

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2023-07-27
Est. Completion 2023-11-17
Phase NA

What the finished NCT06571058 record still lists

NCT06571058 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 5 interventions - of which Questionnaire Administration is the first listed.

NCT06571058 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06571058 about?

NCT06571058 is a clinical study titled "B3 Buddy for Securing Urinary Drainage Bag to Patient While Walking". This clinical trial tests how well the Bag Below Bladder (B3) Buddy device works in securing urinary drainage bags while walking. Keeping a urinary drainage bag below the bladder is the standard of care to maintain urine flow and prevent urine from backing up into the bladder. Despite the use of mod...

What is the current status of trial NCT06571058?

This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2023-07-27. Estimated completion is 2023-11-17.

What interventions are being tested in trial NCT06571058?

The interventions under investigation include: Questionnaire Administration (OTHER), Medical Device Usage and Evaluation (OTHER), Educational Intervention (OTHER), Medical Device Usage and Evaluation (DEVICE), Assistance (OTHER).

Who is sponsoring clinical trial NCT06571058?

This trial is sponsored by Ohio State University Comprehensive Cancer Center, which has 341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06571058's enrollment target sits among peer trials

41 1446th of 2000 higher than 554 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03449238 · 41 participants · Phase 1

    Pembrolizumab And Stereotactic Radiosurgery (Srs) Of Selected Brain Metastases In Breast Cancer Patients

  • NCT03900793 · 41 participants · Phase 1

    Losartan + Sunitinib in Treatment of Osteosarcoma

  • NCT04082520 · 41 participants · Phase 2

    Lutathera for the Treatment of Inoperable, Progressive Meningioma After External Beam Radiation Therapy

  • NCT04220190 · 41 participants · Phase 2

    RAPA-501 Therapy for ALS

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06571058, the US trial registry maintained by the National Library of Medicine. NCT06571058 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.