Cranfixer

Clinical Trial of Cranfixer

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190528043740N1

Enrollment

Registered

2019-06-07

Start date

2018-02-15

Completion date

Unknown

Last updated

2019-08-26

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

Conditions

Flap Fixation instrument (Burr Hole Cover). Mechanical complication of internal fixation device of other bones

Interventions

Intervention group: Cranfixer.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Neurosurgery that leads to the separation of the skull's flap

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Skull Flap Loosining. Timepoint: At least 6 month after surgery. Method of measurement: Qualitative Study (Touch).;Infection. Timepoint: 2 to 4 weeks after surgery. Method of measurement: Infection detection.	—

Secondary

Measure	Time frame
Non-Touchable from The skin. Timepoint: At least 6 month after surgery. Method of measurement: Qualitative Study (Touch).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Roholah Ghodsi

Darman Afarin Noandish Afagh

roholahghodsi@gmail.com+98 21 8338 4167

Outcome results

None listed

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