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To Compare Anaesthetic Effect of intrathecal 1% 2-Chloroprocaine versus ropivacaine 0.5% with Fentanyl in Urological Surgeries.

Comparison Of Anaesthetic Effect of intrathecal 1% 2-Chloroprocaine versus ropivacaine 0.5% with Fentanyl in urological surgeries:A Randomized double blind, interventional study, SMS Medical College and Attached group of Hospitals,Jaipur during 2020-2021.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/037980
Enrollment
60
Registered
2021-11-12
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: N399- Disorder of urinary system, unspecified

Interventions

Intervention1: Group A: 30 patients will receive intrathecal 1% 2-chloroprocaine with fentanyl. Control Intervention1: Group B: 30 patients will receive intrathecal 0.5% ropivacaine with fentanyl.

Sponsors

Department of Anaesthesiology SMS Medical College and Attached Group of Hospitals Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients willing to give consent to participate in the study. 2.Patients posted for urological surgeries belonging to ASA grade I and II. 3.Age between 18 and 55 years. 4.Weight between 50 and 75 kg and height between 150 and 180 cms.

Exclusion criteria

Exclusion criteria: 1.Patients with skin infection at local site. 2.Patients with severe hypovolemia, severe MS, blood coagulopathies. 3.Patients with raised intracranial pressure. 4.Patients allergic to drugs used for study. 5.Failure of spinal anaesthesia, cases in which general anaesthesia will be required.

Design outcomes

Primary

MeasureTime frame
To compare the difference in mean onset time and duration of motor block in both groups.Timepoint: To compare the difference in mean onset time and duration of motor block in both groups.

Secondary

MeasureTime frame
1.To compare the in degree of motor and sensory block in both groups. 2.To determine difference in change in hemodynamic variables for baseline to 5,10,15,20 mins upto 4 hours post spinal period. 3. Adverse effects if any.Timepoint: Time taken from intrathecal injection to achieve highest level of sensory block and modified bromage score 1 to 4 hours post op to check complications if any.

Countries

India

Contacts

Public ContactDr Aayushi Dadhich

S.M.S. Medical College and Attached Group Of Hospitals

vkothari66@gmail.com9414870228

Outcome results

None listed

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