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Clinical Trials/NCT00273715
NCT00273715CompletedPhase 4

A Comparative Randomized Efficacy Study of Sutures Versus Staples in Hip Surgical Procedures

University of Kentucky1 site in 1 country93 target enrollmentStarted: December 1, 2005Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
93
Locations
1
Primary Endpoint
Amount of drainage from skin closure site

Study Overview

Brief Summary

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

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Arms & Interventions

Staples

No Intervention

Intervention: Surgical wound closure techniques (Procedure)

Staples

No Intervention

Intervention: Surgical wound closure techniques (Comparator) (Procedure)

Outcomes

Primary Outcomes

Amount of drainage from skin closure site

Time Frame: up to 5 days following surgery

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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