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Use of 3D printing to help treat heel bone fractures

3D printing assisted reduction and internal fixation for calcaneal fractures - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/095920
Enrollment
40
Registered
2025-10-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: S920- Fracture of calcaneus

Interventions

Intervention1: 3D printing–assisted reduction and fixation of fractured calcaneum bone: Patients with intra-articular displaced calcaneal fractures planned for operative management will be randomized

Sponsors

AIIMS Intramural grant
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with acute, closed, displaced, Sanders type II, III or IV unilateral or bilateral calcaneal fracture without associated ipsilateral lower limb injury.

Exclusion criteria

Exclusion criteria: 1.Patients with previous history of ankle or foot surgery. 2.Pathological fractures, open fractures, severe soft tissue injuries (Tscherne and Oestern closed grade II and grade III). 3.Patients with existing ipsilateral ankle or foot deformity. 4.Patients not giving consent for the study.

Design outcomes

Primary

MeasureTime frame
Operative time (in minutes) for surgical fixation of intra-articular calcaneal fracturesTimepoint: Measured intraoperatively at the time of surgery for each patient (single time point)

Secondary

MeasureTime frame
Number of intraoperative fluoroscopy exposures (C-arm shots) used during fixation of calcaneal fracturesTimepoint: Measured intraoperatively during the surgery for each patient (single time point);Radiographic parameters – Böhler’s angle, Gissane’s angle, calcaneal height, & calcaneal widthTimepoint: Immediately postoperative (within 1 week after surgery) & at final follow-up (6 months postoperatively);Functional outcome evaluated by the American Orthopaedic Foot & Ankle Society (AOFAS) Ankle–Hindfoot Score & Visual Analogue Scale (VAS) for painTimepoint: At 6 weeks, 3 months, & 6 months postoperatively

Countries

India

Contacts

Public ContactAsjad Mahmood

Jai Prakash Narayan Apex Trauma Centre, AIIMS, New Delhi

mahmoodasjad@gmail.com9968856990

Outcome results

None listed

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