Study of Sutures Versus Staples for Skin Closure After Surgical Procedures of Hip

NCT ID: NCT00273715

Last Updated: 2013-07-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

93 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-12-31

Study Completion Date

2008-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Skin closure either by sutures or staples is required after any surgical procedure of the hip.

The purpose of this study is to compare the amount of drainage between patients who have had either staples or sutures placed for skin closure.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Skin closure either by sutures or staples is required after any surgical procedure of the hip.

The purpose of this study is to compare the amount of drainage between patients who have had either staples or sutures placed for skin closure.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Staples

Group Type NO_INTERVENTION

Surgical wound closure techniques

Intervention Type PROCEDURE

Subjects will be randomized to either receive sutures or staples during the surical procedure to close the incision

Surgical wound closure techniques (Comparator)

Intervention Type PROCEDURE

Subjects will be randomized to either receive sutures or staples during the surical procedure to close the incision

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Surgical wound closure techniques

Subjects will be randomized to either receive sutures or staples during the surical procedure to close the incision

Intervention Type PROCEDURE

Surgical wound closure techniques (Comparator)

Subjects will be randomized to either receive sutures or staples during the surical procedure to close the incision

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* The patient must be 18 years of age or greater
* The patient must need an operative procedure of hip

Exclusion Criteria

* Patients who are unable to undergo surgery.
* Patients who have a history of clotting or bleeding abnormalities.
* Patients who have arthroscopic hip surgery.
* Patients who have infections.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Kentucky

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jeffrey Selby, MD

Role: PRINCIPAL_INVESTIGATOR

University of Kentucky Department of Orthopaedic Surgery

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Kentucky Chandler Medical Center

Lexington, Kentucky, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

05-0715-F2L

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Suture Closure Trial
NCT05261425 ACTIVE_NOT_RECRUITING NA
Closure of Appendicular Stump
NCT07229690 COMPLETED