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NCT Number: NCT06407180

Efficacy of Intra-Articular Corticosteroid Injections on Clinical Outcomes in Patients With Operative Distal Radius Fractures

The randomized controlled study which compare clinical outcomes (functional score) in patients with distal radius fractures who underwent open reduction with internal fixation and received intra-articular steroid injections to those who received placebo injections.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Randomization of Patients for Intra-articular Triamcinolone Injection

Objective: To compare the effectiveness of intra-articular Triamcinolone injection versus placebo in patients with distal radius fractures who underwent open reduction with internal fixation

Methods:

Patients: Patients with distal radius fractures who need open reduction with internal fixation procedure Randomization: Patients will be randomly assigned to one of two groups using a block randomization procedure with a block size of 4. Randomization will be performed using STATA version 16.0 software.

Interventions:

Group 1: Patients in this group will receive an intra-articular injection of 10 mg Triamcinolone (1 ml) during surgery.

Group 2: Patients in this group will receive an intra-articular injection of 1 ml normal saline solution during surgery.

Allocation Concealment:

A central randomization service will prepare sealed envelopes containing the assigned treatment for each patient.

The envelopes will be labeled with the patient's name and study ID. The envelopes will be kept in a secure location until the time of surgery.

Blinding:

The study participants, surgeons, and assessors will be blinded to the treatment allocation.

The syringes will be covered with an opaque glove material to further conceal the treatment allocation.

Outcome Measures:

Pain scores Function scores(PRWE score : Patient-Rated Wrist Evaluation) Wrist range of motion Grip strength

Follow-up:

Patients will be followed up at 2 weeks, 6 weeks, 3 months, and 6 months after surgery.

Statistical Analysis:

Demographic Analysis

Analyze the differences in each demographic factor between the groups. For continuous data, use Mean and Standard Deviation (S.D.). For categorical data, use Number, Percentage, and Chi-square. Inferential Statistics

Compare the results of the study, including:

Postoperative pain scores Wrist function score (PRWE) Wrist circumference (mm) Wrist grip strength (kg) Use Mean and S.D. for continuous data. Use Mixed linear model for data analysis. Use STATA 16.0 software for statistical calculations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age more than 18 years old
  • Closed unstable distal radius fracture unstable type which need surgical management
  • Received procedure ORIF with plate and screws at injured wrist

Exclusion criteria

  • History of corticosteroid allergy
  • Poor Diabetes controlled (HbA1C) > 8
  • Who need Ritonavir while enter this study
  • Unable to follow up until the end of projects
  • Unable to do questionnaires
  • Infection around injured wrist
  • Tear tendon at injured wrist
  • Open fracture of injured wrist

Treatment and study plan

Triamcinolone Acetonide

Drug

receive intraarticular triamcinolone injection

normal saline

Drug

receive intraarticular normal saline injection

Primary outcomes

  1. Patient-Rated Wrist Evaluation Score

    Time frame: 12 months

    (0-100) Higher scores mean poorer functional outcome

Secondary outcomes

  1. Visual Analog Scale:

    Time frame: 12 months

    (0-10) Higher scores mean more pain

  2. Grip strength (kg)

    Time frame: 12 months

    Measure by hand dynamometer

  3. Wrist circumference

    Time frame: 12 months

  4. ROM of wrist

    Time frame: 12 months

    range of motion

Study contacts

Contact information is provided by the study sponsor or research team.

Teeradon Waewworawit, Doctor of medicine

CONTACT

[email protected]

(+66)928347744

Thanat Charoenpol, Diploma of Orthopaedics

CONTACT

(+66)02-201-1589

Sponsors and collaborators

Lead sponsor

Teeradon Waewworawit

Other

Registry information

Official study title

Efficacy of Intra-Articular Corticosteroid Injections on Clinical Outcomes in Patients With Operative Distal Radius Fractures: A Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
May 9, 2024
Registry last updated
May 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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