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A Comparative Assessment Of Motor recovery Profile Following Spinal Anaesthesia With doses Of 0.5% Bupivacaine Versus 0.75% Ropivacaine In Perineal Surgeries

Assessment Of Ambulatory Profile Following Spinal Anaesthesia With Equipotent doses Of 0.5% Bupivacaine Versus 0.75% Ropivacaine In Perineal Surgeries- A Comparative Study - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062503
Enrollment
100
Registered
2024-02-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: K602- Anal fissure, unspecified Health Condition 2: O- Medical and Surgical Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: 0.5% Hyperbaric Bupivacaine: 1.5ml Of 0.5% Hyperbaric Bupivacaine with 20 mcg Fentanyl given intrathecally at L3-L4 space using 27G Pencan Needle Control Intervention1: 0.75 % Hyperbar

Sponsors

Kadhij FathimaM
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All ASA I, II and III patients planned for Perineal Surgeries under Spinal Anaesthesia 2. Duration of surgery less than 2 hours

Exclusion criteria

Exclusion criteria: 1. Patient refusal 2. Patients who are categorized above ASA III 3. Patients with Spine deformities 4. Patients with known allergies to Local Anaesthetics and Fentanyl 5. Patients with known neurological, psychiatric and vestibular disease

Design outcomes

Primary

MeasureTime frame
Time of return of ambulation after spinal anaesthesiaTimepoint: At baseline, at the end of surgery, and every 15 minutes post operatively until patient is able to walk without assistance

Secondary

MeasureTime frame
1.Unassisted Sitting 2.Unassisted Standing 3.Negative Rhombergs sign Timepoint: Time for unassisted sitting unassisted standing Negative Rhombergs test to be achieved after administration of spinal anaesthesia is assessed & compared between two groups at the end of surgery & every 15 minutes postoperatively until patient is able to walk without asssistance

Countries

India

Contacts

Public ContactAkilandeshwari

Sri Ramachandra Institute Of Higher Education And Research

akilaanes@gmail.com9840636238

Outcome results

None listed

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