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NCT05657990 · ClinicalTrials.gov registry record · Early Phase 1

Post Operative Urinary Retention (POUR) Following Thoracic Oncological Surgery

A Early Phase 1 study of Urinary Retention, sponsored by Hackensack Meridian Health.

Recruiting
Registry status
Early Phase 1
Development phase
46
Enrollment target
4
Study locations

NCT05657990: Recruiting Early Phase 1 study of Urinary Retention, sponsored by Hackensack Meridian Health.

NCT05657990 is a Early Phase 1 study of Urinary Retention that is actively recruiting participants, run by Hackensack Meridian Health. The registered enrollment target is 46 participants, below the 136-participant average among 11 other Urinary Retention trials with a reported enrollment target (66% lower). The trial reports 4 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05657990, a Early Phase 1 study of Urinary Retention, is actively recruiting participants, sponsored by Hackensack Meridian Health.

RECRUITING
Registry status
Early Phase 1
Development phase
46 participants
Enrollment target
4
Study locations

Study Summary

This is a feasibility study looking at whether the use of Tamsulosin could lower the high incidence of postoperative urinary retention (POUR) in older men who undergo an oncological thoracic surgical procedure for suspected or confirmed cancer. In addition, the study will try to identify the time of resumption of presurgical urinary function post Tamsulosin administration.

Primary Outcome

Self-reported void within 6-8 hours post operative

Conditions Studied

Interventions

  • DRUG Tamsulosin

Study Locations (4)

New Jersey

  • Ocean University Medical Center - Brick
  • South Ocean University Medical Center - Manahawkin
  • Jersey Shore University Medical Center - Neptune City
  • Riverview Medical Center - Red Bank

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2023-04-03
Est. Completion 2026-12
Phase Early Phase 1
Hackensack Meridian Health

90 total trials

What NCT05657990 shows while recruiting

NCT05657990 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 136-participant average among 11 other Urinary Retention trials with a reported enrollment target (66% lower).

The record links to 1 condition, with Urinary Retention appearing as the primary indexed condition, and to 1 intervention - of which Tamsulosin is the first listed.

NCT05657990 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT05657990 about?

NCT05657990 is a clinical study titled "Post Operative Urinary Retention (POUR) Following Thoracic Oncological Surgery". This is a feasibility study looking at whether the use of Tamsulosin could lower the high incidence of postoperative urinary retention (POUR) in older men who undergo an oncological thoracic surgical procedure for suspected or confirmed cancer. In addition, the study will try to identify the time of...

What is the current status of trial NCT05657990?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 46 participants. The study started on 2023-04-03. Estimated completion is 2026-12.

What conditions does trial NCT05657990 study?

This clinical trial studies the following conditions: Urinary Retention.

What interventions are being tested in trial NCT05657990?

The interventions under investigation include: Tamsulosin (DRUG).

Who is sponsoring clinical trial NCT05657990?

This trial is sponsored by Hackensack Meridian Health, which has 90 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05657990 being conducted?

This trial has 4 study locations across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Urinary Retention

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05657990's enrollment target sits among peer trials

46 9th of 11 higher than 3 of 11 other Urinary Retention trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Urinary Retention 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

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Source: ClinicalTrials.gov NCT05657990, the US trial registry maintained by the National Library of Medicine. NCT05657990 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.