Comparision of duration of sensory block in Hyperbaric Bupivacaine and Hyperbaric Ropivacaine in Spinal anaesthesia For Vaginal Hysterectomy

Comparative Evaluation of 0.5% Hyperbaric Bupivacaine and 0.75% Hyperbaric Ropivacaine in patient undergoing Vaginal Hysterectomy under sabarachnoid block - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/082442

Enrollment

106

Registered

2025-03-17

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Health Condition 1: N710- Acute inflammatory disease of uterus

Interventions

Intervention1: Spinal Anaesthesia : Duration of Sensory Block compared between 0.5% Hyperbaric Bupivacaine and 0.75% Hyperbaric Ropivacaine under Subarachnoid Block Control Intervention1: Intrathecal

Eligibility

Inclusion criteria

Inclusion criteria: Patients with ASA grade I-II,scheduled for Elective Vaginal Hysterectomy under Subarachnoid Block

Exclusion criteria

Exclusion criteria: Patient refusal,Patient with coagulopathies,any specific disease with absolute contraindications of spinal anaesthesia,hypothyroidism or diabetic neuropathy and psychiatric disorder/disease and history of allergic reaction to study drugs

Design outcomes

Primary

Measure	Time frame
Duration of sensory blockTimepoint: Up to 3 hours post operatively	—

Secondary

Measure	Time frame
Duration of analgesiaTimepoint: Upto 6 hour	—

Countries

India

Contacts

Public ContactDr Renuka Damor

RNT Medical College Udaipur Rajasthan

htungaria@gmail.com9829370866

Outcome results

None listed

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