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Clinical Trials/CTRI/2024/07/071583
CTRI/2024/07/071583
Not yet recruiting
Phase 4

Comparative Analysis of 3D Printed Reduction Splints vs Conventional Methods in Zygomaticomaxillary Complex Fractures: Assessing Anatomical Reduction and Clinical Outcomes

Dr Poojalekshmi M B1 site in 1 country16 target enrollmentStarted: August 12, 2024Last updated:

Overview

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Dr Poojalekshmi M B
Enrollment
16
Locations
1
Primary Endpoint
Precision of anatomical reduction assessed by radiographs, measuring orbital

Overview

Brief Summary

“Comparative Analysis of 3D Printed Reduction Splints vs Conventional Methods in Zygomaticomaxillary Complex Fractures: Assessing Anatomical Reduction and Clinical Outcomes -  A Pilot Randomised controlled trial is a double blinded clinical trial provisionally approved by Institute Ethics Committee, yet to start with recruiting participants. The primary objective of my study is “To compare the precision of anatomical reduction in Zygomaticomaxillary Complex fractures between patients treated with a 3D printed reduction splint and those treated with conventional reduction methods” for that will be utilizing the benefits of virtual surgical planning in the treatment planning and procedure of ZMC fractures for providing the best results for the patient. Assessing the effectiveness of this technology in zygomaticomaxillary complex fractures can contribute to advancing surgical techniques and patient care. Improved anatomical reduction and stability may lead to better clinical outcomes, including reduced complications, improved functionality, and enhanced aesthetic results. Positive outcomes from this study could influence and shape clinical guidelines, encouraging the adoption of 3D printing and virtual surgical planning in managing facial fractures.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
15.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients diagnosed with unilateral Zygomaticomaxillary Complex (ZMC) fractures confirmed through clinical examination and imaging (CT scans).
  • Adults aged 15 to 65 years.
  • Willingness to provide informed consent for participation in the study.
  • Patients within 1 month from the occurrence of ZMC fracture v.
  • Absence of prior history of zygomaticomaxillary complex fractures.

Exclusion Criteria

  • Patients with bilateral Zygomaticomaxillary Complex fractures.
  • Inability or unwillingness to complywith studyrequirements, including scheduled follow-up visits.
  • Pregnant individuals due to potential risks associated with imaging procedures and treatment iv.
  • Inability to understand or communicate effectively in the language used for study assessments.
  • Severe medical conditions that may impact the ability to undergo surgery or participate in the study.
  • Syndromes with malar involvement: Eg., Malar hypoplasia in Treacher-Collins Syndrome.

Outcomes

Primary Outcomes

Precision of anatomical reduction assessed by radiographs, measuring orbital

Time Frame: Preoperatively, Immediate post operatively, One week post operatively, One month post operatively and Three months post operatively

volume and linear dimensions.

Time Frame: Preoperatively, Immediate post operatively, One week post operatively, One month post operatively and Three months post operatively

Secondary Outcomes

  • 1. Facialsymmetry and aesthetic outcomes assessed through clinical photography(in both frontal and supracranial oblique view.)

Investigators

Sponsor
Dr Poojalekshmi M B
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

POOJALEKSHMI M B

ALL INDIA INSTITUTE OF MEDICAL SCIENCES RAIPUR

Study Sites (1)

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