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prolonged duration of Levobupivacaine with fentanyl for inguinal hernia repair

TO COMPARE THE EFFICACY OF FENTANYL AS AN ADJUWANT TO INTRATHECAL HYPERBARIC LEVOBUPIVACAINE FOR INGUINAL HERNIORRHAPHY:A PROSPECTIVE RANDOMIZED DOUBLE BLIND TRIAL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/10/006239
Enrollment
60
Registered
2015-10-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system Health Condition 2: null- Patients undergoing inguinal herniorrhaphy

Interventions

Intervention1: to study effects of intrathecal hyperbaric levobupivacaine group L: Spinal anesthesia will be performed in the lateral position with midline approach at theL3â??L4 intervertebral spac

Sponsors

INDIRA GANDHI EMPLOYEES STATE INSURANCE HOSPITAL JHILMIL DELHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patients undergoing inguinal herniorrhaphy

Exclusion criteria

Exclusion criteria: Patients with other co-morbid conditions History of drug hypersensitivity to local anaesthetics Blood coagulation disorders Unwilling patients Those with spinal deformities Those with raised intracranial tension With local sepsis

Design outcomes

Primary

MeasureTime frame
Duration of sensory block and time to postop analgesia Timepoint: checking pinprick sensation every single minute for 10 minutes, then every 3 min till half hour then 30, 45, and 60 minutes after injection, and then half hourly until sensory regression to L3 level

Secondary

MeasureTime frame
Secondary outcome measures will be â?? highest level of sensory block ,time-to-peak sensory block, 2-segment regression time, regression time to L3 level , time to maximum Bromage score, highest Bromage score, time to rescue analgesia ,side effects such as discomfort, nausea, vomiting, shivering, pruritus and hemodynamic parameters heart rate, mean arterial pressure, arterial oxygen saturation will monitored frequently.Timepoint: half hourly until sensory regression to L3 level and regression of motor block.Patients will be monitored postop for side effects till stay in recovery ward

Countries

India

Contacts

Public ContactDR SEEMA KALRA

IGESI HOSPITAL,JHILMIL DELHI

kalraseema1965@gmail.com09810960596

Outcome results

None listed

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