Badr University in Cairo (BUC)
Cairo, Cairo Governorate, 12311, Egypt
NCT Number: NCT06510673
PURPOSE: To compare the effect of Extracorporeal shock wave therapy and high-power LASER therapy for the treatment of patients with calcaneal spur Background: Calcaneal spur is a common musculoskeletal disorder of the foot that affect the quality-of-life Conservative treatment modalities include, cold application, platelet-rich plasma therapy (PRP), shoe modification, therapeutic ultrasound, extracorporeal shock wave therapy (ESWT), laser therapy (LLLT) are commonly used in the treatment of calcaneal spur.
HYPOTHESES: There will be difference between Extracorporeal shock wave therapy and High- power LASER therapy on pain intensity in patients with calcaneal spur There will be difference between Extracorporeal shock wave therapy and High- power LASER therapy on function in patients with calcaneal spur. There will be difference between Extracorporeal shock wave therapy and High- power LASER therapy on the size of calcaneal spur in patients with calcaneal spur.
RESEARCH QUESTION: Is there any difference between the effect of Extracorporeal shock wave therapy and High-power LASER on calcaneal spur?
Looking for future studies?
Notify Me25 year–40 year
All sexes
Interventional
Not applicable
Cairo, Cairo Governorate, 12311, Egypt
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
diagnosed with calcaneal spur based on clinical examination and radiological findings.
Exclusion criteria
were as follows: acute trauma to the foot, history of fracture or surgery, lower extremity neurological deficit, polyneuropathy, radicular pain, autoimmune diseases tumor, thrombosis, soft tissue or bone infection, or skin disorder.
Platelet-rich plasma for the heel
High power LASER sessions for the heel
Shockwave therapy sessions for the heel
Sham LASER for the heel
Time frame: Baseline and after one month
It is a self reported outcome which is a 10 cm line with zero at one end indicating no pain and 10 at the other end indicating maximum pain. Patient will be asked to mark the current pain on the scale and the distance from the starting point (0) will be measured
Time frame: Baseline and after one month
measure the impact of foot pathology on function in terms of pain, disability and activity restriction. it is a self-administered index
Time frame: Baseline and after one month
Spur length will be measured by MRI
Cairo University
Other
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.
Published trials that share one or more normalized conditions with this study.
NCT07463794
Bone Diseases, Calcaneal Spur
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT06533683
Bone Diseases, Calcaneal Spur
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT04836845
Bone Diseases, Calcaneal Spur
Van, Turkey (Türkiye)
View Trial DetailsNCT03907085
Bone Diseases, Calcaneal Spur
Afyonkarahisar, Eyalet/Yerleşke, Turkey (Türkiye)
View Trial Details