About this trial
The goal of this clinical trial is to learn if placental growth factor injection and platelet rich plasma injection works to treat peripheral nerve injury in adults. and the role of nerve conduction study and neuromuscular ultrasound
The main questions it aims to answer are:
Does placental growth factor improve outcome after peripheral nerve injury? Does platelet rich plasma improve outcome after peripheral nerve injury? Researchers will compare drug both drugs to each other and will follow up the results via NCS and NMUS
Participants will be classified into 3 random groups:
one group will receive perineural injection of placental growth factor, the other group will receive peri neural PRP injection, third group will only be followed up without intervention Follow up of each patients will be done at 3 and 6 months
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult patients older than 16 yrs old.
Patients with traumatic median or ulnar nerve injury who are complaining of symptoms or functional disability.
Patients with these injuries for more than 3 months
Disqualifiers
1- Presence of other causes of nerve affection (entrapment, Diabetes, etc).
Trial design
Parallel
Treatments tested in this trial
perineural injection
Drugperineural intervention of placental growth factor in one group and PRP in other group
Treatment groups
Trial outcomes
Primary outcomes
efficacy of placental growth factor injection guided by ultrasound and nerve conduction
pre and post injection follow up will be done my measuring the nerve conduction velocity and amplitude , and by determining the cross sectional area of the nerve by ultrasound
efficacy of platelet rich plasma injection guided by ultrasound and nerve conduction
pre and post injection parameters of nerve conduction as velocity and amplitude will be measured as will as parameters of ultrasound such as cross sectional area
Secondary outcomes
diagnosis and follow up of patients by nerve conduction study and neuromuscular US
patients will undergo baseline NCS and NMUS and then follow up the outcome of injection at 3 and 6 months the following parameters will be measured : nerve conduction velocity and amplitude as well as cross sectional area of the nerve
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: