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Comparison of intra operative blood loss between percutaneous pedicle screw fixation kinimally invasive decompression laminectomy and open screw fixation with decompressive laminectomy, in traumatic spine fracture with spinal cord injury

Comparison of intra operative blood loss between percutaneous pedicle screw fixation kinimally invasive decompression laminectomy and open screw fixation with decompressive laminectomy, in traumatic spine fracture with spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20260711010
Enrollment
36
Registered
2026-07-11
Start date
2022-01-01
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

Comparison of intraoperative blood loss between percutaneous pedicle screw fixation with minimally invasive decompressive laminectomy and open screw fixation with decompressive laminectomy, in traumatic spine fracture with spinal cord injury percutaneous pedicle screw fixation with minimally invasive decompressive laminectomy, open screw fixation with decompressive laminectomy, traumatic spine fracture with spinal cord injury

Interventions

Patients underwent Percutaneous Pedicle Screw fixation combined with Minimally Invasive Decompressive laminectomy,Patients underwent traditional Open Screw fixation with decompressive laminectomy
Health Services Research,Health Services Research
PSMD Group (Experimental),OS Group (Comparator)

Sponsors

Prapokklao Hospital
Lead Sponsor
Suppakron Srisumrit,Tavechai Jirachuphun,Rachata O-anuruk
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 to 65 years 2.Fracture classification of AO Type A3, B, or C 3.acute neurological deficits 4.surgical intervention performed within 14 days of the traumatic event. 5.presentation with traumatic fractures at the thoracolumbar junction

Exclusion criteria

Exclusion criteria: 1.Patients with severe cardiopulmonary comorbidities that precluded safe anesthesia or significantly altered recovery 2.Pathological fractures resulting from spinal tumors, metastases, or tuberculosis 3. Evidence of old fractures or pre-existing degenerative conditions at the same spinal level 4. Patients with osteoporotic compression fractures.

Design outcomes

Primary

MeasureTime frame
Intraoperative Blood Loss Intraoperative Quantified in milliliters (mL) by calculating the total volume collected in the suction canister during the procedure—

Secondary

MeasureTime frame
Cobb angle pre-operative, post operative measurements on lateral X-rays,operative time Intraoperative timing,Power Score Pre-operative, 12-Week Follow-up physical examination,Length of hospitalization total days from admission to discharge timing—

Countries

Thailand

Contacts

Public ContactDr. Witthawat Homcharoen

Department of Orthopedics, Prapokklao Hospital

petch_1210@hotmail.com0818085888

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026