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Genetics in high blood pressure patients

Genetic Study of Circadian Locomotor Output Cycle Kaput (CLOCK) Gene Polymorphism in Essential Hypertension - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/091563
Enrollment
180
Registered
2025-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: I10- Essential (primary) hypertension

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

BLDE Deemed to be University Shri B M Patil Medical College Hospital and Research Centre
Lead Sponsor
Dr VINEETH MURALEEDHARAN NAIR
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients Admitted or Attending OPD With Essential Hypertension

Exclusion criteria

Exclusion criteria: 1. Patients with Secondary Hypertension. 2. Patients with Renal Disorders. 3. Patients with Thyroid Disorders.

Design outcomes

Primary

MeasureTime frame
To Identify the Individual Risk of CLOCK Gene Mutation in Patients with Essential HypertensionTimepoint: 12 months

Secondary

MeasureTime frame
This study will be helpful to development of biomarkers to the clinician and the community. By using the study s aggregated data for early detection of essential hypertension and early intervention, the burden of disease in terms of morbidity and mortality of disease will be reduced.Timepoint: 12 MONTHS

Countries

India

Contacts

Public ContactDr. Badiger Sharanabasawappa

BLDE Deemed to be University Shri B M Patil Medical College, Hospital and Research Centre

sharanrb@rediffmail.com9448434927

Outcome results

None listed

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