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A clinical trial to study the effect of patients own platelet-rich plasma injection compared to standard treatment on pain and recovery in acute lateral ankle sprain.

Autologous Platelet-Rich Plasma (PRP) For The Treatment Of Acute Lateral Ankle Sprain: A Randomized Control Study - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/0106020
Enrollment
60
Registered
2026-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: M70-M79- Other soft tissue disorders

Interventions

Intervention1: Autologus Platelet Rich Plasma injection will be given.: Ultrasound guided injection of Autologus Platelet Rich Plasma will be given to injured anterior tall-fibular ligament in a patei

Sponsors

All India Institute of Medical Sciences, Jodhpur,
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18 55 years of either gender, 2. First-time lateral ankle sprain with duration of injury less than48 hours

Exclusion criteria

Exclusion criteria: 1.Lateral ankle sprain injury duration more than 48 hours 2.Patients aged less than 18 years 3.History of previous ankle injury, patients 4. Evidence of infection at the injection site 5.Patients with a history of peripheral vascular disease 6.patient on anticoagulation treatment 7.Patient who is pregnant and lactating female 8.Patients having diabetes 9.Neurological or psychiatric disorders 10.Patient not willing to give written informed consent.

Design outcomes

Primary

MeasureTime frame
1. To compare the ankle function based on the AOFAS score at the time of admission, 4, 8, and 24 weeks 2. To compare the quality of ATFL based on MRI scan using the SNR value at 4 and 24 weeks. Timepoint: Baseline at first presentation then at 4 weeks, 8 weeks, and at 24 weeks

Secondary

MeasureTime frame
1. To compare the pain on VAS score at 0, 7 days, 2 weeks, 4 weeks, 8 weeks, & 24 weeks. 2. Lower Extremity Functional Scale (LEFS) 0, 4, 8, & 24 weeks. 3. To compare the Foot & ankle disability index (FADI) at 0, 4, 8, & 24 weeks. Timepoint: At day 0, 1 week, 2 weeks, 4 weeks, 8 weeks, & at 24 weeks.

Countries

India

Contacts

Public ContactDr Rajesh Kumar Rajnish

All India Institute of Medical Scinces, Jodhpur

rajnishrk@aiimsjodhpur.edu.in9650736850

Outcome results

None listed

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