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dextrose injection platelet rich plasma injection for the treatment of heel pain.

"USG GUIDED DEXTROSE PROLOTHERAPY VERSUS PLATELET-RICH PLASMA INJECTIONS FOR THE TREATMENT OF PLANTAR FASCIITIS:A RANDOMIZED CONTROLLED TRIAL"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035572
Enrollment
56
Registered
2021-08-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M722- Plantar fascial fibromatosis

Interventions

Intervention1: GROUP A: The subjects of this group will receive 25% Dextrose Prolotherapy with 2% 1ml of lignocaine.: â?¢The subjectâ??s will be placed in prone position with feet hanging over edge o

Sponsors

KGMU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 18-60 Years. 2.Idiopathic plantar fasciitis 3.Patient with clinically confirmed diagnosis of the plantar fasciitis refractory to conservative treatment of 2 weeks. 4.Subject willing to participate in the study

Exclusion criteria

Exclusion criteria: 1.Patient refusal to take part in study 2.Acute trauma of ankle and foot 3.Fracture or stress fracture of calcaneum 4.Acute infection (cellulitis, local abscess, septic arthritis) 5.Open wound over heel •Osteomyelitis of calcaneum •Entrapment neuropathy •Previous surgery of plantar fascia •The patient will excluded if they received local steroid injection within 1 month. •Non- steroidal anti-inflammatory drugs or acetylsalicylate with in 72 hours. •Patient with Hb- •Platelet count less than 150,000 per microliter of blood •Uncontrolled diabetes mellitus •Malignancy

Design outcomes

Primary

MeasureTime frame
â?¢Clinical parameter â?¢Assessment of pain-pain relief score (PRS) â?? baseline, 3rd and 6th weeks after injection â?¢Assessment of disability-foot functional index (FFI), foot and ankle outcome score (FAOS) â?? baseline 3rdand 6th weeks after injection Timepoint: at 0, 3rd week and 6th week

Secondary

MeasureTime frame
foot and ankle outcome scoreTimepoint: 0, 3rd , 6th weeks

Countries

India

Contacts

Public ContactDr Sudhir R Mishra

King George medical university

neelam000927@gmail.com9455868708

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026