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Compare chloroprocaine and bupivacaine in caesarean section

A comparative study of intrathecal isobaric 2-Chloroprocaine 1% with hyperbaric Bupivacaine 0.5% in patient undergoing lower segment caesarean section.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018342
Enrollment
60
Registered
2019-03-29
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: O- Medical and Surgical

Interventions

Intervention1: Spinal anasthesia in caesarean section: Duration of study is around one year Control Intervention1: Compare 1% chloroprocaine and 0.5% bupivacaine: Comparison between 1% chloroprocaine

Sponsors

Department of anaesthesiology Jln Medical College ajmer
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient age between 18 â?? 80 years. 2.ASA physical status 1 and 2.

Exclusion criteria

Exclusion criteria: 1.Age 80 years. 2.ASA physical status 3,4,5 and 6. 3.Patients refusal. 4.Patient sensitive / allergic to local anaesthetic agents. 5.Patients with peripheral sensorineural deficit. 6.Patients on anticoagulants. 7.Infection at the site of of lumbar puncture.

Design outcomes

Primary

MeasureTime frame
To determine duration of analgesia of chloroprocaine after intrathecal useTimepoint: Duration of study is around one year

Secondary

MeasureTime frame
Onset of motor blockade Onset of sensory blockade Duration of sensory blockade Duration of motor blockade â?¢ Two segment regression. â?¢ Complications like nausea, vomiting, hematoma, intravascular injections, local anaesthetic toxicity, bradycardia (50 bpm), hypotension (decrease in SBP30% baseline or 100mm Hg).Timepoint: Duration of study is around 1 year

Countries

India

Contacts

Public ContactDr Neena jain

Jln Medical College ajmer

drneenaj@gmail.com9414008666

Outcome results

None listed

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