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Calcaneal SpurNCT06510673

Effect of Extracorporeal Shockwave Therapy, High Power-LASER & Platelet-rich Protein on Pain and Function in Patients With Calcaneal Spur A Randomized Comparative Study.

A study testing Platelet rich plasma, High power LASER and Shockwave therapy in people with Calcaneal Spur, run by Cairo University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 25 to 40 years
Conditions the study is for
Calcaneal Spur
What is being tested?
Platelet rich plasma, High power LASER and Shockwave therapy
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
96 participants
Where
1 siteEgypt
Study dates
1 Oct 2024to 1 Jun 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • diagnosed with calcaneal spur based on clinical examination and radiological findings.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Badr University in Cairo (BUC)

    Cairo, Cairo Governorate, 12311

Other trials in Egypt

About this study

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?

Conditions
Calcaneal Spur
Being tested
Platelet rich plasma, High power LASER, Shockwave therapy, Sham LASER
Medical subject headings
Heel Spur

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Platelet rich plasmaDrug

    Platelet-rich plasma for the heel

  • High power LASEROther

    High power LASER sessions for the heel

  • Shockwave therapyOther

    Shockwave therapy sessions for the heel

  • Sham LASEROther

    Sham LASER for the heel

Study groups in NCT06510673
Study groupRoleWhat they receive
Shockwave therapyExperimentalShockwave therapy for calcaneal spur
Receives: Other: Shockwave therapy
High-power LASER therapyExperimentalHigh-power LASER therapy for calcaneal spur
Receives: Other: High power LASER
ControlSham comparatorcold application with receive 6 sessions of sham LASER therapy.
Receives: Other: Sham LASER
Platelet rich plasmaExperimentalPlatelet-rich plasma injection for the heel
Receives: Drug: Platelet rich plasma

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain Visual Analog Scale

    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

    Measured: Baseline and after one month

  2. foot function index.

    measure the impact of foot pathology on function in terms of pain, disability and activity restriction. it is a self-administered index

    Measured: Baseline and after one month

  3. calcaneal Spur length

    Spur length will be measured by MRI

    Measured: Baseline and after one month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Jul 2024
  2. Study start1 Oct 2024
  3. Primary completion1 Apr 2025
  4. Study completion1 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
96 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06510673
Sponsor's protocol ID
SU1
Status last verified
Aug 2024
First submitted
15 Jul 2024
Last updated
12 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Platelet rich plasma, High power LASER and Shockwave therapy in people with Calcaneal Spur, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain Visual Analog Scale (time frame: Baseline and after one month). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Jun 2026; AzTrials last refreshed its copy on 7 Nov 2026.

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