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Determining optimal Co-load volume using point of care ultrasonography to prevent post spinal anaesthesia hypotension.

Determining optimal Co-load volume using point of care ultrasonography to prevent post spinal anaesthesia hypotension - An observational study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/075173
Enrollment
30
Registered
2024-10-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

None listed

Interventions

Intervention1: nil: nil

Sponsors

Dr Neelima Ganne
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1 and 2 Absence of any systemic illness Absence of renal diseases Surgery not lasting for than three hours

Exclusion criteria

Exclusion criteria: Patient with history of CVS,RS,ENDOCRINE,NEUROLOGICAL,RENAL and HEPATIC disease. Patients with history of cardiac disease who has Ejection fraction less than 45%. Patients with pulmonary hypertension. History of hypotension. Pregnant patients. Emergency surgeries Contraindications for spinal anaesthesia

Design outcomes

Primary

MeasureTime frame
To determine optimal co-load volume to prevent post spinal hypotension.Timepoint: 3,6,9,12,15,20,25,30,35,40,45,50,55,60 minutes after spinal anaesthesia—

Secondary

MeasureTime frame
not applicableTimepoint: not applicable—

Countries

India

Contacts

Public ContactDr Chaitanya A Kamat

Jawaharlal Nehru Medical college

drchaitanya12@gmail.com8150038305

Outcome results

None listed

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