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Comparison between two drugs with additives in spinal anaesthesia for surgeries below the umbilicus.

Comparison between Hyperbaric Bupivacaine with Fentanyl and Hyperbaric Levobupivacaine with Fentanyl in spinal anaesthesia for infraumbilical surgeries- a hospital based randomized controlled trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062670
Enrollment
100
Registered
2024-02-15
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: O- Medical and Surgical

Interventions

Intervention1: Hyperbaric Bupivacaine with Fentanyl: Spinal anaesthesia is the most common anaesthesia procedure for patients undergoing surgeries for below the umbilicus level. It is most commonly do

Sponsors

Dr Jennifer Konsam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients undergoing infraumbilical surgeries under spinal anaesthesia. 2.ASA grade I and II. 3.Patients willing to give informed consent.

Exclusion criteria

Exclusion criteria: 1.Hypersensitivity to any of the drugs under study. 2.Non-consenting or unable to give consent. 3.Patients with any contraindication to spinal anaesthesia. 4.Patients who do not fulfill the inclusion criteria.

Design outcomes

Primary

MeasureTime frame
To compare the onset and duration of sensory and motor blockade between 0.5% Hyperbaric Bupivacaine with 25mcg Fentanyl and 0.5% Hyperbaric Levobupivacaine with 25mcg Fentanyl for spinal anaesthesia in patients undergoing elective infraumbilical surgeries.Timepoint: From the time of drug administration till upto 4 hours.

Secondary

MeasureTime frame
To study the hemodynamic changes.Timepoint: From the time of drug administration till upto 4 hours.

Countries

India

Contacts

Public ContactJennifer Konsam

Jawaharlal Nehru Medical College

mallappadhorigol@gmail.com9844778096

Outcome results

None listed

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