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The study to compare efficacy and safety of divided doses spinal anaesthesia drug with single dose of spinal anaesthesia drug for elderly patient undergoing vaginal hysterectomy

Prospective observational study to compare efficacy and safety of fractionated dose verses single bolus dose in spinal anesthesia for elderly patients undergoing vaginal hysterectomy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/12/078019
Enrollment
60
Registered
2024-12-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: N814- Uterovaginal prolapse, unspecified

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil Control Intervention2: Nil: Nil

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient posted for elective vaginal hysterectomy Expected duration of surgery is less than 4hrs Patient is able to give informed written consent

Exclusion criteria

Exclusion criteria: Any contraindications for spinal anaesthesia Inability to understand or comply with the study protocol

Design outcomes

Primary

MeasureTime frame
To compare hemodynamics changes To compare incidence of hypotensionTimepoint: From the injection of spinal drug to end of surgery—

Secondary

MeasureTime frame
To compare vasoactive drug required to treat hypotension intra operative To compare failure of spinal anaesthesia.Timepoint: From the injection of spinal drug to 24 hr post surgery—

Countries

India

Contacts

Public ContactDr Jyoti magar

Department of anaesthesiology LTMMC & GH Sion hospital Mumbai,India

jyotimagar2110@gmail.com9833706466

Outcome results

None listed

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