Faculty of Medicine Ramathibodi Hospital, Mahidol University
Ratchathewi, Bangkok, 10400, Thailand
NCT Number: NCT06678568
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.
Trial opening soon.
Get NotifiedUp to 12 year
All sexes
Interventional
Not applicable
Ratchathewi, Bangkok, 10400, Thailand
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:
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intervention group will be appointed with telemedicine follow-up in 3rd week after injury, instead of hospital follow-up visit.
Time frame: From enrollment to the end of treatment at 4 weeks
Angulation is more than 10 degree in coronal view or more than 20 degree in sagittal view
Time frame: From enrollment to the end of treatment at 4 weeks
Number of Participants with malunion, nonunion, joint stiffness and cast problem
Contact information is provided by the study sponsor or research team.
Chanika Angsanuntsukh, Diploma of orthopaedics
CONTACT
(+66)917767879
Nonticha Thanthong, Doctor of medicine
CONTACT
(+66)898829505
Nonticha Thanthong
Other
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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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