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A clinical study to find out incidence of blood clot formation in high risk patients undergoing spine surgery.

A Prospective,cross sectional study to find out incidence of deep vein thrombosis in high risk patients undergoing spine surgery. - No

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2014/09/004949
Enrollment
250
Registered
2014-09-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: null- Deep Vein Thrombosis in High risk patients undergoing spine Surgery

Interventions

None listed

Sponsors

Stavya Spine Hospital and Research Institute
Lead Sponsor
Stavya Spine Hospital and Research Institute
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients are included in the study if they are undergoing spine surgery at Stavya Spine Hospital and Research Institute with any of the following criteria: 1.Malignancy: present or past within 6 months 2.Hematological disorder (Thrombophilia, High factor VIII levels, antithrombin deficiency, protein c deficiency, protein s deficiency, high fibrinogen levels, high factor IX levels, high factor XI levels, leukemia, thrombocytosis) 3.Immobilisation- 72 hours 4.Past history of DVT 5.Varicose veins 6.Spine infection 7.Obesity (BMI > 30) 8.Age > 65 years 9.Myelopathy with Nurickâ??s Grade 3 or more than 3 10.ASIA Impairment scale (AIS) grade A/B/C 11.Long duration of surgery > 2 hours

Exclusion criteria

Exclusion criteria: Patients are excluded from participating in this study if any of the following criteria are met: 1.Patient not fulfilling inclusion criteria 2.Patient not willing to participate in the study or not willing to sign the consent form. 3.Active local infection of lower limb like cellulitis. 4.Active hepatitis (receiving medical treatment within two years); 5.Pregnant or planning to become pregnant during study period; 6.Patients who have limited life expectancy due to significant medical comorbidities. 7.Known or documented history of communicable disease, including AIDS or HIV; 8.Immunologically suppressed, history of Pagetâ??s disease, osteomalacia, or any other metabolic bone disease; 9.Active hepatitis (receiving medical treatment within two years)

Design outcomes

Primary

MeasureTime frame
Positive venous color doppler study of lower limbs for diagnosing deep vein thrombosis.Timepoint: The assessment will be made preoperatively on admission and approximate 6 weeks after surgery—

Secondary

MeasureTime frame
NilTimepoint: Nil—

Countries

India

Contacts

Public ContactDr Shaunak C Dudhia

Stavya Spine Hospital and Research Institute

drajaykrishnan@yahoo.co.in07926565657

Outcome results

None listed

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