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Comparison of intrathecal fentanyl with isobaric ropivacaine v/s isobaric levobupivacaine(two different anaesthetic agents) for lower abdominal surgery under subarachnoid block:A prospective double blind randomized study

Comparison of intrathecal fentanyl with isobaric ropivacaine v/s isobaric levobupivacaine for lower abdominal surgery under subarachnoid block:A prospective double blind randomized study - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069120
Enrollment
50
Registered
2024-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: - Health Condition 2: R688- Other general symptoms and signs

Interventions

Intervention1: Inj isobaric levobupivacaine(0.5%) with fentanyl: patients in Group LB will receive inj isobaric levobupivacaine(0.5%) 2.5cc with fentanyl 25mcg(0.5ml) using 23G/25G Quinckes spinal nee

Sponsors

government medical college bhavnagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients undergoing lower abdominal surgery and willing to give consent 2)Age group 20-60 years 3)Patients with ASA grade I/II/III

Exclusion criteria

Exclusion criteria: 1)History of allergy to local anaesthetic drugs 2)Patients with history of bleeding disorders 3)Patients having spinal abnormalities like spina bifida or meningocele 4)Incraesed ICP

Design outcomes

Primary

MeasureTime frame
Onset and duration of sensory as well as motor blockade and duration of analgesiaTimepoint: 30min 60min 120min—

Secondary

MeasureTime frame
1)To determine the changes in hemodynamic parameters and oxygen saturation 2)To see for side effects of subarachnoid block in both groups if anyTimepoint: 18 months—

Countries

India

Contacts

Public ContactDr Komal Shah

Government medical college Bhavnagar

shah.komal@rediffmail.com9427215252

Outcome results

None listed

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