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NCT02652611 · ClinicalTrials.gov registry record · NA

Sacroiliac (SI) Screws: The Effect of SI Screw Removal on Patient-Reported Pain and Functional Outcomes

A NA study, sponsored by University of Maryland, Baltimore.

Completed
Registry status
NA
Development phase
60
Enrollment target

NCT02652611 is a NA study that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 60 participants.

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The verdict

NCT02652611, a NA study, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

Chronic pain following surgical stabilization of a pelvic fracture is very prominent and can have a major affect on a patient's quality of life. Persistent pain after radiographic evidence of fracture union commonly leads to implant removal. But, the routine removal of orthopaedic fixation devices after fracture healing remains an issue of debate.

Interventions

  • PROCEDURE SI Screw Removal Surgery
  • PROCEDURE Non-screw removal treatment (non-operative management)

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2015-09
Est. Completion 2020-12
Phase NA

Sponsor

University of Maryland, Baltimore

560 total trials

What the Registry Record Tells You About NCT02652611

The ClinicalTrials.gov registry entry for NCT02652611 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Maryland, Baltimore, which has 560 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which SI Screw Removal Surgery is the first listed.

NCT02652611 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02652611 about?

NCT02652611 is a clinical study titled "Sacroiliac (SI) Screws: The Effect of SI Screw Removal on Patient-Reported Pain and Functional Outcomes". Chronic pain following surgical stabilization of a pelvic fracture is very prominent and can have a major affect on a patient's quality of life. Persistent pain after radiographic evidence of fracture union commonly leads to implant removal. But, the routine removal of orthopaedic fixation devices a...

What is the current status of trial NCT02652611?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2015-09. Estimated completion is 2020-12.

What interventions are being tested in trial NCT02652611?

The interventions under investigation include: SI Screw Removal Surgery (PROCEDURE), Non-screw removal treatment (non-operative management) (PROCEDURE).

Who is sponsoring clinical trial NCT02652611?

This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.