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The Optimized Follow-up Protocol for Pediatric Metaphyseal Forearm Fractures

The Optimized Follow-up Protocol for Pediatric Metaphyseal Forearm Fractures

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06678568
Enrollment
72
Registered
2024-11-07
Start date
2024-11-05
Completion date
2026-12-31
Last updated
2024-11-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wrist Fracture

Keywords

metaphyseal forearm fracture, loss of reduction, follow-up protocol, wrist fracture

Brief summary

The randomized controlled study which compare radiologic outcomes (loss of reduction rate) and complications in pediatric patients with displaced metaphyseal forearm fractures who underwent conservative treatment. The patients were assigned in two different follow-up protocols. In the control group, the patients will go to hospital for follow-up visit and film every week until 4th week after injury. In the intervention group, the patients will go to hospital for follow-up visit every week except in the 3rd week after injury they will be gotten telemedicine follow-up.

Detailed description

Randomization of patients for 2 different follow-up protocols Objective: to compare loss of reduction rate by angulation measurement and prevalence of complications in patients with displaced metaphyseal forearm fractures who underwent conservative treatment. Method: Patients will be randomly assigned to one of two groups using various block computerized randomization. Randomization will be performed using STATA version 16.0, Statacorp, College Station, Texas, USA Interventions: Group 1 (control group): The patients will go to hospital for follow-up visit and film every week until 4th week after injury. Group 2 (intervention group): The patients will go to hospital for follow-up visit every week except in the 3rd week after injury they will be gotten telemedicine follow-up. Treatment Allocation and concealment: A randomization will prepare with sealed envelopes containing assigned follow-up protocols for each patient. The envelopes will be labeled with the study ID. Blinding: Because of the two different of follow-up protocol, we cannot blind the protocol from participants, physicians and assessors. Outcomes: 1. Primary outcome is loss of reduction rate using angulation measurement. The definition of loss of reduction angulation is angulation which is more than 10 degree in coronal view or more than 20 degree in sagittal view. Angulation measurement will be measured in bisector between longitudinal axis and center of diaphysis. Angulation will be measured by two physicians and two times using PACS (Picture Archiving and Communication System) in Ramathibodi hospital. 2. Secondary outcomes are other complications such as malunion, nonunion, joint stiffness and cast problem Statistical Analysis Plan: Data will be recorded in Microsoft Excel and imported to STATA version 16.0 for re-check. For continuous data, use mean and standard deviation (S.D.) For categorical data, use frequency and percentage For comparing non-normal distribution between group, use Mann-Whitney test and for continuous data, use Fisher's exact test Define the Statistical significant is p-value \< 0.05 Data analysis will be performed with STATA version 16.0, Statacorp, College Station, Texas, USA.

Interventions

OTHERtelemedicine follow-up in 3rd week

Intervention group will be appointed with telemedicine follow-up in 3rd week after injury, instead of hospital follow-up visit.

Sponsors

Nonticha Thanthong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 0-12 years * Patients with distal metaphyseal forearm fractures in Ramathibodi hospital and Chakri Naruebodindra Medical Institute * Presented to hospital within 72 hours of injury

Exclusion criteria

* Open fracture * Operative treatment at 1st visit * Neurovascular injury * Polytraumatized patient * Ipsilateral fracture of upper limb * History of previous surgery in the affected arm * Metabolic bone disease

Design outcomes

Primary

MeasureTime frameDescription
loss of reduction rateFrom enrollment to the end of treatment at 4 weeksAngulation is more than 10 degree in coronal view or more than 20 degree in sagittal view

Secondary

MeasureTime frameDescription
ComplicationsFrom enrollment to the end of treatment at 4 weeksNumber of Participants with malunion, nonunion, joint stiffness and cast problem

Countries

Thailand

Contacts

Primary ContactNonticha Thanthong, Doctor of medicine
por-43@hotmail.co.th(+66)898829505
Backup ContactChanika Angsanuntsukh, Diploma of orthopaedics
achanika@gmail.com(+66)917767879

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026