LIMIT: Lateralization After IntraMedullary Nailing of InterTrochanteric Hip Fractures, Clinical and Radiographic Outcomes

Sponsor
Prisma Health-Upstate (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05094791
Collaborator
Arthrex, Inc. (Industry)
60
1
12
5

Study Details

Study Description

Brief Summary

Intertrochanteric fractures are commonly stabilized using an intramedullary nail with a lag screw that enters the lateral cortex of the femur. This lag screw commonly protrudes during the healing process and may cause implant related pain. This study will help determine if implant related pain is different depending to the lag screw design.

Condition or Disease Intervention/Treatment Phase
  • Device: Telescoping Lag Screw
  • Device: Standard lag Screw
  • Device: Standard lag screw with addition of worm screw

Detailed Description

This study compares cephalomedullary fixation of intertrochanteric femur fractures using the Arthrex Hip Nail System with a telescoping lag screw compared to the Zimmer Natural Nail and the Smith and Nephew InterTan. This pilot study will evaluate radiographic outcomes and lateral sided hip pain related to different lag screw designs used for patients with intertrochanteric femur fractures by comparing outcomes of patients receiving 3 different lag screws The primary objective of this study is to compare pain at the level of the lag screw of patients with collapsible lag screws compared to patient who received a standard lag screw using a numeric rating scale on a 0-100 scale.

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Lateralization After IntraMedullary Nailing of InterTrochanteric Hip Fractures, Clinical and Radiographic Outcomes
Actual Study Start Date :
Oct 4, 2021
Anticipated Primary Completion Date :
Oct 4, 2022
Anticipated Study Completion Date :
Oct 4, 2022

Arms and Interventions

Arm Intervention/Treatment
Telescoping Lag Screw

Intertrochanteric fractures treated with Arthrex Hip Nail with Telescoping Screw

Device: Telescoping Lag Screw
Intertrochanteric fracture fixation using Arthrex Hip Nail with Telescoping Lag Screw
Other Names:
  • Arthrex Hip Nail
  • Standard lag Screw

    Intertrochanteric fractures treated with Zimmer Natural Nail Cephalomedullary Nail

    Device: Standard lag Screw
    Intertrochanteric fracture fixation using Zimmer Natural Nail Cephalomedullary Nail using standard lag screw
    Other Names:
  • Zimmer Natural Nail
  • Standard lag screw with addition of worm screw

    Intertrochanteric fractures treated with Smith and Nephew TRIGEN INTERTAN

    Device: Standard lag screw with addition of worm screw
    Intertrochanteric fracture fixation using Smith and Nephew TRIGEN INTERTAN with addition of worm screw
    Other Names:
  • Smith and Nephew TRIGEN INTERTAN
  • Outcome Measures

    Primary Outcome Measures

    1. Pain at lag screw [6 weeks]

      Pain will be accessed at the location of the lag screw, pain will be measured by using a Numeric rating scale (0-100)

    2. Pain at lag screw [12 weeks]

      Pain will be accessed at the location of the lag screw, pain will be measured by using a Numeric rating scale (0-100)

    3. Pain at lag screw [21 weeks]

      Pain will be accessed at the location of the lag screw, pain will be measured by using a Numeric rating scale (0-100)

    4. Pain at lag screw [52 weeks]

      Pain will be accessed at the location of the lag screw, pain will be measured by using a Numeric rating scale (0-100)

    Secondary Outcome Measures

    1. Radiographic lateralization of lag screw [52 weeks]

      Change in the lateralization of the lag screw measured in mm

    2. Incidence of lag screw injections [52 weeks]

      Incidence of patients requiring injections at the location of the lag screw due to pain

    3. Reoperation rate [52 weeks]

      Reoperations to the location in the intertrochanteric fractue

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    22 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients greater than or equal to 22 years of age who undergo treatment of an intertrochanteric hip fracture with an intramedullary nail.

    • Fluoroscopic views of the final fixation construct or a post-operative radiograph taken within 24 hours must be available.

    Exclusion Criteria:
    • Non-ambulatory prior to injury (patient must do more than only transfers)

    • Cognitive deficiencies that prevent the patient from providing their own informed consent

    • Inability to follow-up at the discretion of the investigator (incarceration, moving out of area, no permanent housing)

    • Prior fracture to injured hip

    • Prior surgery to injured hip

    • Basi-cervical fracture pattern (fracture that begins above the lesser trochanter and exits medial to the greater trochanter)

    • Patients not treated within 48 hours of admission

    • Chronic or acute infection at site of surgery

    • Language barrier preventing completion of study forms in English

    • Open fracture

    • Fracture related to neoplasm

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Greenville Memorial Hosptial Greenville South Carolina United States 29605

    Sponsors and Collaborators

    • Prisma Health-Upstate
    • Arthrex, Inc.

    Investigators

    • Principal Investigator: John D Adams, MD, Prisma Health

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Prisma Health-Upstate
    ClinicalTrials.gov Identifier:
    NCT05094791
    Other Study ID Numbers:
    • Pro00113048
    First Posted:
    Oct 26, 2021
    Last Update Posted:
    Oct 26, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 26, 2021