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Outcome of a Less Invasive Spine Stabilization Surgery in 47 Patients

Inter-muscular postero-lateral minimal invasive open approach revisited: Spectrum of possibilities and Outcomes of stabilization. A retrospective observational study of 47 patients. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/104106
Enrollment
47
Registered
2026-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: M532- Spinal instabilities

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Stavya Spine Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Traumatic fractures 2. Fragility fracture 3. Pathological fractures of different etiology, infective spondylodiscitis and metastasis/primary tumour 4. Patients who were poorer and couldn t afford a percutaneous screws system and neither wanted to pursue the subsidised health schemes.

Exclusion criteria

Exclusion criteria: 1. Patients with incomplete records 2. Previously operated at same/adjacent levels 3. Patients presented with other co-existing spinal regions/ joints/ metabolic/ congenital/ diseases that could significantly influence the outcome of the patient.

Design outcomes

Primary

MeasureTime frame
1. All the patients were assessed thoroughly and demographic details (age, sex, BMI), primary diagnosis, pre-operative neurology (ASIA grading), classification of disorder, and spinal region were recorded. 2.To evaluate intra operative parameters in form of estimated blood loss ,duration of surgery & intra operative time for screw placement 3.To evaluate post operative parameters inn the form of length of hospital stay, requirement of post operative analgesia ,post op complications (if any)Timepoint: Baseline, intra-operative, and follow-up data at 3 months, 6 months, 12 months, and 24 months are required.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Ajay Krishnan

Stavya Spine Hospital And Research Institute

drajaykrishnan@yahoo.co.in09824302768

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026