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Investigating the effect of adding platelet-enriched plasma (PRP) injection to exercise chronic ankle sprain

Investigating the effect of adding platelet-enriched plasma (PRP) injection to exercise therapy on pain and balance in patients with chronic ankle sprain

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180205038619N3
Enrollment
30
Registered
2025-07-15
Start date
2024-07-12
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Ankle sprain. Sprain of ankle

Interventions

Intervention 1: Intervention group: Blind Platelet-rich plasma(PRP)+exercise therapy. Intervention 2: Control group: Exercise therapy.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Informed consent Age between 18 and 60 years At least 3 months of similar pain At least one episode of ankle giving-way after an initial sprain Grade 2 anterior talofibular ligament (ATFL) injury (incomplete ligament tear, partial loss of functional mobility, and mild to moderate joint instability) and Grade 3 injury (complete ligament tear, inability to bear weight or significant joint instability, in which the patient’s pain decreases with initial conservative treatments including relative rest, cryotherapy, bandaging, elevation, and immobilization). VAS score greater than 4

Exclusion criteria

Exclusion criteria: Musculoskeletal disorders (e.g., genu varum/valgum, flatfoot, high arches) History of ankle surgery or trauma Steroid injection or other interventions within past 6 months Pregnancy History of Diabetes Mellitus History of cancer Occurrence of a severe complication resulting from the injection Participant withdrawal Ankle pathologies such as cellulitis, cuts, bruises, osteomyelitis, deformities Known rheumatologic diseases (e.g., RA) Anterior talofibular ligament (ATFL) injury requiring surgical intervention (complete ligament tear, inability to bear weight, or significant joint instability in which the patient’s pain does not improve with initial conservative treatments including relative rest, cryotherapy, bandaging, elevation, and immobilization, or when the patient prefers surgical treatment). Inability of the participant to complete follow-up assessments

Design outcomes

Primary

MeasureTime frame
The severity of pain. Timepoint: Zero, one month, 3 months, six months after. Method of measurement: Visual Analog Scale (VAS).;Function of ankle in daily life and sport activities according to FAAM questionnaire. Timepoint: Zero, one month, 3 months, six months after. Method of measurement: Foot and Ankle Ability Measure (FAAM) questionnaire.;Results of Biodex System which is in Firoozgar hospital. Timepoint: Zero, one month, 3 months, six months after. Method of measurement: Biodex Balance system.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKatayoun Moradi

Iran University of Medical Sciences

katayounmoradi69@gmail.com0098 021 64351

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026