A clinical trial of porous titanium implants for better integration.
Not Applicable
- Conditions
- Health Condition 1: R900- Intracranial space-occupying lesion found on diagnostic imaging of central nervous system
- Registration Number
- CTRI/2022/01/039175
- Lead Sponsor
- DRDO Ministry of Defence Government of India
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
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
Pregnant women and child. Patient not willing to be part of trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Infection, Hematoma formation, accurate integration of burr hole buttonTimepoint: 1 6 & 12 Month
- Secondary Outcome Measures
Name Time Method patient health condition before and after surgeryTimepoint: 3 Month <br/ ><br>9 month