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Evaluation of anticoagulant usage against Deep vein clot in patients with blood clot in the brain â??A Prospective observational study

Evaluation of anticoagulant usage against Deep Vein Thrombosis in patients with spontaneous intracranial hemorrhage â??A Prospective observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/09/009716
Enrollment
300
Registered
2017-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Spontaneous Intracranial hemorrhage

Interventions

Control Intervention1: 1. LMWH SQ Clexane 0.6 ml once daily OD and low dose Aspirin or Ecospirin 150mg OD. 2. Low dose Aspirin or Ecospirin 150mg OD: Patients visiting for consultation with diagnosis

Sponsors

Kasturba medical college Kasturba Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients newly diagnosed with SICH confirmed by coronary tomography (CT) or magnetic resonance imaging (MRI) scans. Patients of both gender, 18 yrs and above. Patients prescribed with either monotherapy (low dose aspirin) or dual therapy (SQ LMWH + Low dose aspirin).

Exclusion criteria

Exclusion criteria: Patients on previous anticoagulant therapy. No available imaging studies, including initial coronary tomography angiography (CTA). Patients previously treated with SICH in another hospital. Patients who are unwilling to participate in the study.

Design outcomes

Primary

MeasureTime frame
Study exposure variables: â?¢ D-dimer values or ultrasound. Primary outcome measures: DVT and pulmonary embolism. Timepoint: Clinical data collection during the hospital stay and follow up at 3 weeks, 3 months and 6 months during the study period.

Secondary

MeasureTime frame
Study exposure variables - Blood pressure (BP) measurement. Coagulation tests including platelet count, PT, APTT, and INR. Study outcome variables â?? CT Scan- Hematoma volume expansion leading to a major SICH. The abrupt onset of focal neurological symptoms such as vomiting, systolic BP 220 mmHg, severe headache, coma or decreased level of consciousness. Prognosis of ICH severity scale estimating an all cause 30-day mortality. Timepoint: Clinical data collection during the hospital stay and follow up at 3 weeks, 3 months and 6 months during the study period.

Countries

India

Contacts

Public ContactSravani Velicheti

Manipal College of Pharmaceutical sciences

nair.sreedhar@manipal.edu9844545682

Outcome results

None listed

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