Assessing the Effects of Hyperbaric vs. Isobaric Ropivacaine for Abdominal Surgeries Using Thoracic Spinal Anesthesia

Evaluation of intrathecal hyperbaric versus isobaric ropivacaine for abdominal surgeries under thoracic spinal anaesthesia a comparative study - NIL

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/076179

Enrollment

Registered

2024-11-04

Start date

Unknown

Completion date

Unknown

Last updated

2024-12-09

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: Thoracic spinal anaesthesia: Thoracic spinal anaesthesia with hyperbaric Ropivacaine(0.75%) with Fentanyl Control Intervention1: Thoracic spinal anaesthesia: Thoracic spinal anaesthesia

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 18 to 65 years 2.American Society of Anesthesiologists physical status I-II 3.Scheduled for elective abdominal surgeries 4.Height: =140cm 5.Weight: 40kg - 70kg

Exclusion criteria

Exclusion criteria: 1.Patient refusal. 2.Patient with a.Coagulopathies or on anticoagulant medication b.Any specific disease includes severe cardiopulmonary disease, blood volume deficit, diabetic or other peripheral neuropathies, neurological deficit and severe hepatic renal disease c.Psychiatric disorder 3.History of allergic reaction to study drugs

Design outcomes

Primary

Measure	Time frame
Onset of sensory block and peak sensory levelTimepoint: time till peak sensory level achieved upto 10 min	—

Secondary

Measure	Time frame
1.Duration of motor & sensory 2.Hemodynamic changes 3.Adverse effects / complications Timepoint: Duration of motor & sensory block up to 6 hours post opratively	—

Countries

India

Contacts

Public ContactDr Mamta Damor

Medical college dungarpur

vineeta7goda@gmail.com8114425535

Outcome results

None listed

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