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This study was conducted to use and determine efficacy of isobaric drug levobupivacaine administered via spinal anesthesia in laparoscopic surgeries

Efficacy of isobaric intrathecal levobupivacine in laproscopic procedures : Case series - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068386
Enrollment
20
Registered
2024-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: K80-K87- Disorders of gallbladder, biliary tract and pancreas Health Condition 2: Z00-Z99- Factors influencing health status and contact with health services

Interventions

Intervention1: Efficacy of isobaric intrathecal levobupivacine in laproscopic procedures : Case series : To determine efficacy of isobaric levobupivacaine in laparoscopic surgeries

Sponsors

Mahatma Gandhi medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patient aged 18-65 years. 2 American Society of Anaesthesiology (ASA) of Classes I/ II 3 Patients undergoing laproscopic surgeries with duration less then 2 hours under spinal anaesthesia. 4 Patients giving consent for study

Exclusion criteria

Exclusion criteria: • Hypersensitivity to study medications • Infection at the site of subarachnoid block • Spinal deformities • Inability to comprehend or participate in pain scoring system • Patient with BMI more then 37kg/m2 • ECG changes like sinus bradycardia and heart blocks • Patient on alpha adrenergic blockers • Contraindication to spinal anaesthesia like bleeding diathesis and local Infection

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy and safety of single shot subarachnoid block Timepoint: Pre-Induction 5 Minutes 10 Minutes 15 Minutes 20 Minutes 25 Minutes 30 Minutes—

Secondary

MeasureTime frame
1 Haemodynamical changes 2 Time to first dose of rescue analgesia 3 Surgeon satisfaction score. 4. Patient satisfaction score Timepoint: Post operativly for 24 hours—

Countries

India

Contacts

Public ContactDr Vigya Goyal

Mahatma Gandhi medical college and hospital

khayyammoin@yahoo.com9468964148

Outcome results

None listed

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