Triamcinolone Acetonide
Drugreceive intraarticular triamcinolone injection
NCT Number: NCT06407180
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.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
receive intraarticular triamcinolone injection
receive intraarticular normal saline injection
Time frame: 12 months
(0-100) Higher scores mean poorer functional outcome
Time frame: 12 months
(0-10) Higher scores mean more pain
Time frame: 12 months
Measure by hand dynamometer
Time frame: 12 months
Time frame: 12 months
range of motion
Contact information is provided by the study sponsor or research team.
Teeradon Waewworawit, Doctor of medicine
CONTACT
(+66)928347744
Thanat Charoenpol, Diploma of Orthopaedics
CONTACT
(+66)02-201-1589
Teeradon Waewworawit
Other
Efficacy of Intra-Articular Corticosteroid Injections on Clinical Outcomes in Patients With Operative Distal Radius Fractures: A Randomized Controlled Trial
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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