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Comparison of conventional and PRP injection in ATFL sprain patients

COMPARISON OF CLINICO-RADIOLOGICAL AND FUNCTIONAL OUTCOMES BETWEEN LOCAL PLATELET RICH PLASMA(PRP) INJECTION VERSUS CONVENTIONAL TREATMENT MODALITY FOR LATERAL ANKLE SPRAIN INJURIES: RANDOMIZED CONTROL STUDY - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096643
Enrollment
34
Registered
2025-10-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: S934- Sprain of ankle

Interventions

Intervention1: PRP INJECTION PATIENTS: All the patients included shall be divided into two groups A and B (17 patients in each group). In group A (control), no injection shall be given at injury site
in group B (Intervention), ONE PRP injection shall be given within 48 hours of the sprain. Autologous PRP injection shall be given under ultrasound guidance to the injured ATFL. Control Intervention1:
in group B (Intervention), ONE PRP injection shall be given within 48 hours of the sprain. Autologous PRP injection shall be given under ultrasound guidance to the injured ATFL. It will be followed by

Sponsors

AIIMS JODHPUR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PATIENT AGED 18-60 YEARS FIRST TIME LATERAL ANKLE SPRAIN DURATION OF INJURY LESS THAN 48 HOURS OF INJURY GRADE 2 MILD TO MODERATE INSTABILITY

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
1. To compare the pain on VAS (Visual Analog Scale) score at 0, 6, and 24 weeks of PRP injection 2. To compare the ankle functional outcomes based on AOFAS score at 0,6, and 24 weeks of PRP injection Timepoint: 0,6,24 WEEKS

Secondary

MeasureTime frame
To compare the Foot & ankle disability index (FADI) at 0, , 6, & 24 weeks of PRP injection Timepoint: 0,6,24 WEEKS;To compare the ankle functional outcomes based on ankle ultrasound scan evaluation at 0,6 and 24 weeks 2.To compare the foot and ankle disability index at 0,2,6,12 and 24 weeksTimepoint:

Countries

India

Contacts

Public ContactRAJESH KUMAR RAJNISH

AIIMS JODHPUR

duktiraj@gmail.com08955444773

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026