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NCT06309368 · ClinicalTrials.gov registry record · Phase 4
Ostomy Primary Closure With 0.1% Betaine/Polyhexanide Wound Irrigation Compared to Pursestring Closure
A Phase 4 study of Surgical Site Infection and Colorectal Disorders, sponsored by University of Nevada, Las Vegas.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 84
- Enrollment target
- 1
- Study location
NCT06309368: Recruiting Phase 4 study of Surgical Site Infection and Colorectal Disorders, sponsored by University of Nevada, Las Vegas.
NCT06309368 is a Phase 4 study of Surgical Site Infection and Colorectal Disorders that is actively recruiting participants, run by University of Nevada, Las Vegas. The registered enrollment target is 84 participants, below the 565-participant average among 25 other Surgical Site Infection trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06309368, a Phase 4 study of Surgical Site Infection and Colorectal Disorders, is actively recruiting participants, sponsored by University of Nevada, Las Vegas.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 84 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to compare two types of closure in patients with ostomies that are ready for closure. The main questions it aims to answer are: 1. Surgical site infection rates 2. Patient quality of life 3. Time to wound healing Participants will undergo either complete ostomy wound closure after washing out the wound with Prontosan, or their ostomy wound will be closed using the Pursestring method, where the wound will be left partially open and allowed to heal from the inside out. Researchers will compare these two groups' outcomes (questions to be answered) as listed above.
Primary Outcome
Evaluate surgical site infection rates between the two treatment arms
Conditions Studied
Interventions
- DRUG Primary Ostomy Closure with 0.1% Betaine/0.1% Polyhexanide Wound Irrigation
- PROCEDURE Pursestring Closure
Study Locations (1)
Nevada
- University Medical Center - Las Vegas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 84 participants |
| Start Date | 2024-03-14 |
| Est. Completion | 2029-12 |
| Phase | Phase 4 |
What NCT06309368 shows while recruiting
NCT06309368 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 84 participants, a relatively small participant target, below the 565-participant average among 25 other Surgical Site Infection trials with a reported enrollment target (85% lower).
The record links to 3 conditions, with Surgical Site Infection appearing as the primary indexed condition, and to 2 interventions - of which Primary Ostomy Closure with 0.1% Betaine/0.1% Polyhexanide Wound Irrigation is the first listed.
NCT06309368 reports a single indexed study location in Nevada.
Frequently Asked Questions
What is clinical trial NCT06309368 about?
NCT06309368 is a clinical study titled "Ostomy Primary Closure With 0.1% Betaine/Polyhexanide Wound Irrigation Compared to Pursestring Closure". The goal of this clinical trial is to compare two types of closure in patients with ostomies that are ready for closure. The main questions it aims to answer are: 1. Surgical site infection rates 2. Patient quality of life 3. Time to wound healing Participants will undergo either complete ostomy w...
What is the current status of trial NCT06309368?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 84 participants. The study started on 2024-03-14. Estimated completion is 2029-12.
What conditions does trial NCT06309368 study?
This clinical trial studies the following conditions: Surgical Site Infection, Colorectal Disorders, Wound Surgical.
What interventions are being tested in trial NCT06309368?
The interventions under investigation include: Primary Ostomy Closure with 0.1% Betaine/0.1% Polyhexanide Wound Irrigation (DRUG), Pursestring Closure (PROCEDURE).
Who is sponsoring clinical trial NCT06309368?
This trial is sponsored by University of Nevada, Las Vegas, which has 52 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06309368 being conducted?
This trial has 1 study location across Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Surgical Site Infection
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 NCT06309368's enrollment target sits among peer trials
84 19th of 25 higher than 7 of 25 other Surgical Site Infection trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Surgical Site Infection 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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