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Comparing 3 different doses of the drug Chlorprocaine in spinal anaesthesia for patients undergoing surgery in the infraumbilical region in terms of duration of effect and ease of ambulation.

A Comparative Assessment Of Duration Of Anaesthesia And Ease Of Ambulation In Patients Undergoing Infraumbilical Procedures Under Sub Arachnoid Block With 3 Different Doses Of 1% Chlorprocaine â?? A Prospective Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034270
Enrollment
60
Registered
2021-06-16
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: Chlorprocaine 3ml in sub arachnoid block: Patients in group A will be given spinal anesthesia with 3 ml of preservative free chlorprocaine Control Intervention1: Chlorprocaine 4 ml in s

Sponsors

R AISHWARYA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I and II patients patients undergoing short duration

Exclusion criteria

Exclusion criteria: Patients with known allergy to local anaesthetic drugs Patients with local infection at the site of injection Patient with coagulopathy and bleeding disorders Contraindications to spinal anaesthesia. History of neuromuscular diseases in the lower extremities. Pregnant and lactating women. Patient refusal

Design outcomes

Primary

MeasureTime frame
Duration of sensory and motor block following spinal anaesthesiaTimepoint: Progression of both sensory and motor blocks evaluated every 2min until readiness for surgery, then every five minutes until the achievement of the maximum level of block and the regression of at least two dermatomes. After that, the assessment of sensory and motor blocks was performed every 30min until complete resolution of spinal block

Secondary

MeasureTime frame
Post operative analgesiaTimepoint: It is assessed at 0,10,20,30, 60 ,90 and 120 min from the end of surgery and then hourly till the next 12 hours.;Readiness for discharge using Modified Aldrete score more than 9Timepoint: Time to reach Aldrete score more than 9 will be recoded post operatively.;Unassisted ambulationTimepoint: Time to reach first unassisted ambulation by standing and walking 3 meters on own.

Countries

India

Contacts

Public ContactR AISHWARYA

Sri Lakshmi Narayana Institute of Medical Sciences

ashirocks1989@gmail.com9953413562

Outcome results

None listed

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