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Hand Incision Study

NCT ID: NCT04656834

Last Updated: 2020-12-07

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

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Recruitment Status

UNKNOWN

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-11-30

Study Completion Date

2021-11-30

Brief Summary

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The cosmetic outcome of a patient's surgical scar is important for patient satisfaction, especially in more visibly exposed areas of the body such as the hand. A patient's surgical scar often serves as a long-term reminder of their surgery experience, so optimizing final scar appearance should be of high importance. Surgical incision closure techniques and suture materials may vary by individual hand surgeons, even with common hand procedures.

Detailed Description

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Conditions

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Hand Surgery

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Hand incision closure type 1

The participating surgeon closes the hand surgical incision via the standard method based on personal preference: buried monocryl sutures and skin glue

hand incision closure using monocryl sutures and skin glue

Intervention Type PROCEDURE

At the end of surgery, the investigator will close the incision using monocryl sutures and skin glue

Hand incision closure type 2

The participating surgeon closes the hand surgical incision via the standard method based on personal preference: simple nylon sutures

hand incision closure using simple nylon sutures

Intervention Type PROCEDURE

At the end of surgery, the investigator will close the incision using simple nylon sutures

Interventions

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hand incision closure using monocryl sutures and skin glue

At the end of surgery, the investigator will close the incision using monocryl sutures and skin glue

Intervention Type PROCEDURE

hand incision closure using simple nylon sutures

At the end of surgery, the investigator will close the incision using simple nylon sutures

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients ≥ 18 years old
* Able to provide consent
* Undergoing either trigger finger release or carpal tunnel release

Exclusion Criteria

* Patients \< 18 years old
* Unable to provide consent
* Unable to comply with follow up requirements
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rothman Institute Orthopaedics

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Rothman Orthopaedic Institute

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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AILY20D.947

Identifier Type: -

Identifier Source: org_study_id