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NCT06615739 · ClinicalTrials.gov registry record

Comprehensive SRS Regenerex Tissue Attachment

A clinical trial of Arthroplasty Complications and Osteo Arthritis Shoulders, sponsored by Zimmer Biomet.

Active
Registry status
22
Enrollment target
1
Study location

NCT06615739: Active study of Arthroplasty Complications and Osteo Arthritis Shoulders, sponsored by Zimmer Biomet.

NCT06615739 is a study of Arthroplasty Complications and Osteo Arthritis Shoulders that is active but no longer recruiting, run by Zimmer Biomet. The registered enrollment target is 22 participants, below the 588-participant average among 5 other Arthroplasty Complications trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06615739, a study of Arthroplasty Complications and Osteo Arthritis Shoulders, is active but no longer recruiting, sponsored by Zimmer Biomet.

ACTIVE NOT RECRUITING
Registry status
22 participants
Enrollment target
1
Study location

Study Summary

The objective of this retrospective and prospective consecutive series data collection is to confirm safety, performance, and clinical benefits of the Comprehensive SRS Regenerex Tissue Attachment Augments when used for limb salvage arthroplasty.

Primary Outcome

This will be established by recording the incidence and frequency of device revisions. Kaplan-Meier survival analysis is a statistical method that estimates survival rates over time and accounts for factors that can affect implant survival.

Interventions

  • DEVICE Regenerex Tissue Attachment Augments

Study Locations (1)

Florida

  • Toman Orthopedics and Sports Med - Boca Raton

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2024-10-22
Est. Completion 2026-12-31
Zimmer Biomet

115 total trials

What the registry record for NCT06615739 still lists

NCT06615739 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 588-participant average among 5 other Arthroplasty Complications trials with a reported enrollment target (96% lower).

The record links to 2 conditions, with Arthroplasty Complications appearing as the primary indexed condition, and to 1 intervention - of which Regenerex Tissue Attachment Augments is the first listed.

NCT06615739 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT06615739 about?

NCT06615739 is a clinical study titled "Comprehensive SRS Regenerex Tissue Attachment". The objective of this retrospective and prospective consecutive series data collection is to confirm safety, performance, and clinical benefits of the Comprehensive SRS Regenerex Tissue Attachment Augments when used for limb salvage arthroplasty.

What is the current status of trial NCT06615739?

This trial is currently active not recruiting. The enrollment target is 22 participants. The study started on 2024-10-22. Estimated completion is 2026-12-31.

What conditions does trial NCT06615739 study?

This clinical trial studies the following conditions: Arthroplasty Complications, Osteo Arthritis Shoulders.

What interventions are being tested in trial NCT06615739?

The interventions under investigation include: Regenerex Tissue Attachment Augments (DEVICE).

Who is sponsoring clinical trial NCT06615739?

This trial is sponsored by Zimmer Biomet, which has 115 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06615739 being conducted?

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

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Source: ClinicalTrials.gov NCT06615739, the US trial registry maintained by the National Library of Medicine. NCT06615739 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.