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Clinical study of Absorbable Bone Wax in Neurological Surgery

Qualitative Assessment of Absorbable Bone Wax in Neurological Surgery

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20151116003
Enrollment
Unknown
Registered
2015-11-16
Start date
2014-01-08
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The ability of new absorbable bone wax in stopping bone bleeding during craniotomy or craniectomy will be evaluated together with the handling properties.

Interventions

Craniotomy or craniectomy is carried out. New absorbable bone wax would be applied to stop bleeding of the bone at the cuttinf edges. Its effciency will be evaluated.
Experimental Device
craniotomy or craniectomy

Sponsors

National Science and Technology Development Agency
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: • Patients who undergo general brain surgery. • Patients who undergo craniotomy or craniectomy or skull surgery which create burr hole. • Patients who have clean wound.

Exclusion criteria

Exclusion criteria: • Patients who have skull infection or osteomyelitis or inflammation • Patients who have blood chemistry which indicated the inflammation i.e higher than normal values of WBC, ESR. • Patients who have opened wound. • Patients who have renal insufficiency or renal failure

Design outcomes

Primary

MeasureTime frame
Hemostasis performance of absorable bone wax Intraoperative Observation

Secondary

MeasureTime frame
Handling properties of absorbable bone wax Intraoperative Manually by hand

Countries

Thaiand

Contacts

Public ContactPataravit Rukskul

hospital medical school affiliations

prukskul@yahoo.com6622926-9523

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026