SPECT-CT Metabolic/Morphological Assessment of Cemented Hip Protheses (SPECT-PROTMA)

March 14, 2022 updated by: Daniel Rodriguez Perez

SPECT-CT Metabolic and Morphological Study of Two Types of Cemented Hip Stem Protheses in Primary Total Hip Arthroplasty Patients: A Randomized Controlled Clinical Trial (SPECT-PROTMA)

Single center, pilot, randomized, controlled clinical trial to assess metabolic and morphological images between two types of cemented stem prostheses in patients undergoing total hip arthroplasty surgery during a 2-year follow up period.

Study Overview

Detailed Description

Single center, pilot, controlled clinical trial to assess metabolic and morphological images of patients undergoing total hip arthroplasty surgery randomized to the thick layer technique (Exeter hip stem model) or to the "French paradox" technique (Müller straight stem model).

Participants will be performed a plain radiography and a SPECT-CT at 3, 6, 12 and 24 months of the intervention. SPECT-CTs will be performed in addition to the usual medical care complementary imaging exams. The SPECT will require the administration of the 99mTechnetium-methylene diphosphonate (99mTc-MDP) radiopharmaceutical (useful to assess bone metabolism) and its combination with a CT scan (SPECT-CT) allows a combined metabolic and morphological study.

Study Type

Interventional

Enrollment (Anticipated)

16

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • patients ≥ 18 years-old
  • both genders
  • patients undergoing a primary total hip arthroplasty surgery with implantation of a cemented prosthesis (Exeter hip stem model or Müller straight stem model)
  • patients with a diagnosis of hip osteoarthritis, operated by the Orthopedic Surgery and Traumatology Department at the Bellvitge University Hospital
  • patients who signed the written informed consent.

Exclusion Criteria:

  • patients allergic to 99mTc-MDP radiopharmaceutical
  • patients with claustrophobia
  • patients with a background of an active septic process
  • patients with a postoperative septic complication
  • patients periprosthetic fracture or misalignment of the prosthetic component
  • patients who have a total hip prosthetic implanted due to a subcapital femoral fracture

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Thick-Layer Technique
Total hip arthroplasty using the Exeter V40 cemented femoral stem [Stryker Orthopaedics, Mahwah, New Jersey].
Consists of applying a cement layer of at least 2 millimeters surrounding an undersized prosthetic stem, so that this layer of cement fits between the femoral medullary canal and the prosthetic's femoral stem.
Other Names:
  • Total hip arthroplasty using the Thick-Layer Technique
Active Comparator: Thin-Layer Technique (French Paradox)
Total hip arthroplasty using the Müller Straight Stem [Zimmer, Winterthur, Switzerland].
Consists of applying a thin layer of cement, so that the prosthetic's femoral stem fills as much as possible the femoral medullary canal.
Other Names:
  • Total hip arthroplasty using the Thin-Layer Technique (French Paradox)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of counts per image set in the SPECT study
Time Frame: 24 months after surgery
Counts per image: unit of measure defined as the number of photons captured by the gamma camera, which represent the radiopharmaceutical uptake
24 months after surgery
Alignment angles in the plain radiography and in the CT scan study.
Time Frame: 24 months after surgery
24 months after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Axial displacement in the plain radiography and in the CT Scan study.
Time Frame: 24 months after surgery
24 months after surgery
Harris Radiographic Classification of Loosening Risk.
Time Frame: 24 months after surgery
24 months after surgery
Harris Hip Score
Time Frame: 24 months after surgery
24 months after surgery
Merle d'Aubigné Score
Time Frame: 24 months after surgery
24 months after surgery
WOMAC Index Score
Time Frame: 24 months after surgery
24 months after surgery
EuroQoL-5D-3L questionnaire score
Time Frame: 24 months after surgery
Permission for this instruments' use has been granted by the EuroQoL Office.
24 months after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Daniel R Pérez, MD, Orthopedic Surgeon Specialized in Hip Arthroplasty

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2022

Primary Completion (Anticipated)

December 31, 2023

Study Completion (Anticipated)

December 31, 2024

Study Registration Dates

First Submitted

August 11, 2021

First Submitted That Met QC Criteria

August 11, 2021

First Posted (Actual)

August 18, 2021

Study Record Updates

Last Update Posted (Actual)

March 15, 2022

Last Update Submitted That Met QC Criteria

March 14, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HUB- COT-2020-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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