Clinical trial to study the action of drug 2-chlorprocaine for loss of pain sensation given through the backbone for lower abdominal operations

A prospective study to evaluate the efficacy of spinal 2-chlorprocaine in infra-umbilical surgeries

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2019/07/020037

Enrollment

Registered

2019-07-04

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: Not applicable: Not applicable Control Intervention1: Not applicable: Not applicable

Eligibility

Inclusion criteria

Inclusion criteria: BMI-19 to 35 kg per cm2, American society of Anesthesiologist grade one,two,three

Exclusion criteria

Exclusion criteria: Infection at the site of spinal,patient on anti coagulant drugs,spinal deformities and patient refusal

Design outcomes

Primary

Measure	Time frame
Adequacy of sensory block which is accessed by two segment regressionTimepoint: Adequacy of sensory block which is accessed by two segment regression till one and half hour	—

Secondary

Measure	Time frame
Complete resolution of sensory block, complete resolution of motor block and micturition timeTimepoint: Assessed from the time of spinal anaesthesia till 4 hours	—

Countries

India

Contacts

Public ContactDr prabu

SKS hospital and post graduate medical institute

gprabu_mmc@yahoo.co.in9884469456

Outcome results

None listed

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