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A study to compare duration of postoperative pain relief for levobupivacaine with or without fentayl in lower abdominal surgeries in spinal anaesthesia.

A prospective Randomised Study To Compare Intrathecal 0.5% Isobaric Levobupivacaine with Or Without Fentanyl 25µg In Various Infraumbilical Surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022353
Enrollment
80
Registered
2019-12-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system

Interventions

Intervention1: Intrathecal block: Duration of analgesia is assessed and duration of study is around 1 year Control Intervention1: 0.5 % isobaric levobupivacaine with or without fentanyl 25 mcg: Campar

Sponsors

JLN Medical college hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to ASA grade 1 & 2 Informed consent

Exclusion criteria

Exclusion criteria: Patient’s refusal. Uncooperative patients. Any contraindication of spinal block. Any known hypersensitivity or contraindication to levobupivacaine and fentanyl. Local pathology at the site of injection or disability limiting the performance of spinal block. Patient with history of respiratory, cardiac, endocrinal, hepatic or renal disease (necessitating classification in ASA Class III or above). Patients having a history of significant neurological, psychiatric, or neuromuscular disorders.

Design outcomes

Primary

MeasureTime frame
Duration of analgesiaTimepoint: 1 year

Secondary

MeasureTime frame
Onset and Duration of sensory block. Onset and Duration of motor block. Peri-operative sedation score Haemodynamic changes if any. Adverse effect/Complication if any Timepoint: 1 year

Countries

India

Contacts

Public ContactDr Veena mathur

Jawahar lal nehru medical college, Ajmer

veenamathur41@gmail.com949460517947

Outcome results

None listed

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