CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 148 enrolled
Drug / intervention
cast +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05521464
NCT05521464N/ACompleted
CompareCT.gov

Robert Jones Bandage Versus Cast in the Treatment of Distal Radius Fracture in Children: a Randomized Controlled Trial

University of Duhok·interventional·Posted Aug 30, 2022·Updated Dec 11, 2023

In Brief

A clinical study evaluating cast and Robert Jones Bandage for Fracture Distal Radius and Children, Only. Completed, enrolled 148 participants across 1 site.

Detailed Summary

Aim and objectives This study aimed to treat fractures of the distal end of the radius in the children with Robert Jones (RJ) bandage in comparison with a cast. The objective was to compare the frequency of occurrence of the complications, child comfortability, and family satisfaction with this treatment modality.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsFracture Distal Radius, Children, Only
CountriesIraq
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedAug 30, 2022
Enrollment StartOct 1, 2021
Primary CompletionAug 20, 2022
Study CompletionAug 21, 2022
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 3.8 years ago

Interventions

castother

Application of a short arm cast from just below the elbow to the finger's knuckles. The cast was from a Plaster of Paris bandage over a cotton pad. The participants who received this treatment modality were considered group 1 (control group)

Robert Jones Bandageother

Modified RJ bandage (firmly applied two layers of bulky cotton layers alternating with two layers of elastic bandage in the following order: bandage - cotton - bandage - cotton - bandage). It was applied from below the elbow to the finger's knuckles. The participants who received this treatment modality were considered group 2 (trial group).