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Comparing prophylactic noradrenaline infusion and phenylephrine infusion after preloading with iv fluids for prevention of fall in blood pressure in elderly patients undergoing proximal femoral nailinig under spinal anaesthesia.

A randomised double blinded study comparing prophylactic noradrenaline infusion and phenylephrine infusion after preloading with crystalloid for prevention of hypotension in geriatric patients undergoing proximal femoral nailinig under spinal anaesthesia. - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064165
Enrollment
60
Registered
2024-03-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Prophylactic infusion of phenylephrine for prevention of hypotension: patient in group A receive phenylephrine infusion at rate of 0.5mcg/kg/min Control Intervention1: Prophylactic infu

Sponsors

Dr Tharigonda Balaji
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA 2 & 3 2.Aged between 65 â?? 80 yrs. 3.Patients posted for PFN surgeries.

Exclusion criteria

Exclusion criteria: 1.Patients with known cardiac abnormalities. 2.Uncontrolled hypertension. 3.Hyperthyroid patients. 4.Coagulation or renal disorders. 5.Infection at the site of spinal anaesthesia

Design outcomes

Primary

MeasureTime frame
Prevention Of Spinal HypotensionTimepoint: heart rate and mean arterial blood pressure at Baseline, every 5 min for first half an hour, every 10 min for next 90 min

Secondary

MeasureTime frame
Adverse events such as bradycardia, nausea and vomiting will be recordedTimepoint: intra operative period and 6 hrs post operatively

Countries

India

Contacts

Public ContactTharigonda Balaji

Government Medical College,Kadapa

meetdrbalaji@gmail.com9491152692

Outcome results

None listed

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