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NCT05805449 · ClinicalTrials.gov registry record · NA

BIOlogic Augmented Repair of Complex Anal Fistula Using Acellular Matrix and/or Autologous Platelet-rich Plasma

A NA study of Anal Fistula, sponsored by The University of Texas Health Science Center, Houston.

Recruiting
Registry status
NA
Development phase
250
Enrollment target
1
Study location

NCT05805449 is a NA study of Anal Fistula that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 250 participants, roughly in line with the 252-participant average among 5 other Anal Fistula trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT05805449, a NA study of Anal Fistula, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.

RECRUITING
Registry status
NA
Development phase
250 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to compare the clinical effectiveness of augmenting surgical repair of complex anal fistula using autologous PRP and/or micronized acellular porcine urinary bladder matrix (UBM) to usual surgical care alone to prevent fistula recurrence or improve HRQoL, to compare the effects of augmenting surgical repair of complex anal fistula using autologous PRP and/or micronized acellular porcine urinary bladder matrix on early postoperative pain and fecal continence and to assess the cost utility of augmented complex fistula repair relative to usual surgical care

Conditions Studied

Interventions

  • PROCEDURE Surgery
  • OTHER Platelet-rich plasma (PRP)
  • DEVICE Matrix

Study Locations (1)

Texas

  • The University of Texas Health Science Center at Houston - Houston

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2023-02-21
Est. Completion 2026-03-31
Phase NA

What the Registry Record Tells You About NCT05805449

The ClinicalTrials.gov registry entry for NCT05805449 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 250 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 252-participant average among 5 other Anal Fistula trials with a reported enrollment target. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Anal Fistula appearing as the primary indexed condition, and to 3 interventions - of which Surgery is the first listed.

NCT05805449 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05805449 about?

NCT05805449 is a clinical study titled "BIOlogic Augmented Repair of Complex Anal Fistula Using Acellular Matrix and/or Autologous Platelet-rich Plasma". The purpose of this study is to compare the clinical effectiveness of augmenting surgical repair of complex anal fistula using autologous PRP and/or micronized acellular porcine urinary bladder matrix (UBM) to usual surgical care alone to prevent fistula recurrence or improve HRQoL, to compare the e...

What is the current status of trial NCT05805449?

This trial is currently recruiting. It is a NA study. The enrollment target is 250 participants. The study started on 2023-02-21. Estimated completion is 2026-03-31.

What conditions does trial NCT05805449 study?

This clinical trial studies the following conditions: Anal Fistula.

What interventions are being tested in trial NCT05805449?

The interventions under investigation include: Surgery (PROCEDURE), Platelet-rich plasma (PRP) (OTHER), Matrix (DEVICE).

Who is sponsoring clinical trial NCT05805449?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05805449 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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