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Comparison of spinal anaesthesia using bupivacaine with fentanyl to spinal anaesthesia using levobupivacaine with fentanyl for transurethral resection of prostate

Comparison of intrathecal bupivacaine with levobupivacaine using fentanyl as an adjuvant for transurethral resection of prostate

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/040873
Enrollment
50
Registered
2022-03-07
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms

Interventions

Intervention1: intrathecal levobupivacaine with fentanyl: intrathecal levobupivacaine isobaric 12.5 mg with fentanyl 25 microgm mixed together single shot by intrathecal route, duration of procedure 1

Sponsors

Deptt of anaesthesia PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male patients undergoing TURP

Exclusion criteria

Exclusion criteria: 1. Patient refusal 2. Local site infection 3. Bleeding disorders 4. Disease of spinal cord, central nervous system 5. Allergy to study drugs

Design outcomes

Primary

MeasureTime frame
time to onset of sensory and motor block in both groups regression of sensory block by 2 segments and complete regression of motor block time to first rescue analgesiaTimepoint: time to onset of sensory and motor block in both groups regression of sensory block by 2 segments and complete regression of motor block time to first rescue analgesia

Secondary

MeasureTime frame
Haemodynamic parameters- heart rate, syatolic BP, diastolic BP, mean arterial pressure need for postoperative analgesia any complications/adverse effects- bradycardia, hypotension, nausea, vomiting, shiveringTimepoint: every 5 min

Countries

India

Contacts

Public ContactSheenam Kamboj

PGIMS Rohtak

mdr.indira@yahoo.in9350224435

Outcome results

None listed

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