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Recruiting NCT06336304

NCT06336304 NXT Post-Market Clinical Follow-up

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Clinical Trial Summary
NCT ID NCT06336304
Status Recruiting
Phase
Sponsor Laborie Medical Technologies Inc.
Condition Urinary Incontinence
Study Type OBSERVATIONAL
Enrollment 180 participants
Start Date 2024-06-18
Primary Completion 2027-03

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Urodynamic procedure

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 180 participants in total. It began in 2024-06-18 with a primary completion date of 2027-03.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

NXT Urodynamics System Post-Market Clinical Follow-up Clinical Investigation to Confirm Ongoing Safety and Performance in Urodynamic Patient Sub-Populations

Eligibility Criteria

Inclusion Criteria: * Patients medically indicated for urodynamic study * Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements Exclusion Criteria: * Patients or legally authorized representative with cognitive or psychiatric condition that interferes with or precludes direct and accurate communication regarding the study, giving informed consent or ability to complete the patient questionnaire * Patients with confirmed active bladder infections (not including patients with asymptotic bacteria) * Pregnant women * Patients with recent (less than 2 weeks) pelvic floor surgery * Requires use of suprapubic catheter

Contact & Investigator

Central Contact

Kaitlyn Palm

✉ rs.nxtpmcf@laborie.com

📞 6128160068

Frequently Asked Questions

Who can join the NCT06336304 clinical trial?

This trial is open to participants of all sexes, studying Urinary Incontinence. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06336304 currently recruiting?

Yes, NCT06336304 is actively recruiting participants. Contact the research team at rs.nxtpmcf@laborie.com for enrollment information.

Where is the NCT06336304 trial being conducted?

This trial is being conducted at Hanover, United States, Owing Mills, United States, Columbus, United States, Columbus, United States and 1 additional location.

Who is sponsoring the NCT06336304 clinical trial?

NCT06336304 is sponsored by Laborie Medical Technologies Inc.. The trial plans to enroll 180 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology