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Follow up in heart vessel surgery

A study on determinants of outcome of coarctation of aorta surgery in paediatric population aimed at the development of feasible follow up strategies.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/10/046366
Enrollment
22
Registered
2022-10-11
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: Q251- Coarctation of aorta

Interventions

None listed

Sponsors

POSTRGADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH, CHANDIGARH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients with symptomatic coarctation of the aorta requiring surgical intervention who consent to be part of the study and follow-up will be included in the study.

Exclusion criteria

Exclusion criteria: Patients who refuses to follow up. Patients/ guardian who refuse to give consent

Design outcomes

Primary

MeasureTime frame
1. Identification of % of patients having re coarctation requiring re intervention. 2. Mean duration between coarctation surgery and re coarctation. 3. % of patients requiring antihypertensive medications in follow up. 4. Risk factors associated with re coarctation based on various variables. 5. Assessment of serum BNP and its use as a marker for symptoms in re coarctation. 6. Histopathological assessment of the coarcted segment.Timepoint: 0, 1, 3, 6, 12 months—

Secondary

MeasureTime frame
NilTimepoint: Nil—

Countries

India

Contacts

Public ContactDR RUPESH KUMAR

Postgraduate institute of medical education and research, Chandigarh

rkctvs@gmail.com9883690388

Outcome results

None listed

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