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A clinical trial of porous titanium implants for better integration.

Customized Bioactive Porous Titanium Implants with improved Tissue-Integration and Attenuated Aseptic Loosening for Orthopaedic Applications.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039175
Enrollment
25
Registered
2022-01-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: R900- Intracranial space-occupying lesion found on diagnostic imaging of central nervous system

Interventions

Intervention1: Porous Titanium burr hole button: Titanium burr hole buttons will be fixed at the untreated region of cranial flap or associate surgery Control Intervention1: NA: NA

Sponsors

DRDO Ministry of Defence Government of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients who undergo craniotomy and left the burr hole defect untreated after the replacement of autologous or engineered cranial flap.

Exclusion criteria

Exclusion criteria: Pregnant women and child. Patient not willing to be part of trial

Design outcomes

Primary

MeasureTime frame
Infection, Hematoma formation, accurate integration of burr hole buttonTimepoint: 1 6 & 12 Month—

Secondary

MeasureTime frame
patient health condition before and after surgeryTimepoint: 3 Month 9 month—

Countries

India

Contacts

Public ContactDr Zahir Quazi

AVBRH, JNMC

s.iratwar@gmail.com

Outcome results

None listed

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