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A clinical trial to compare 1% Chloroprocaine (short acting local anesthetic) in Spinal anesthesia with or without Fentanyl for Enhanced Recovery after Perianal Surgeries

Comparison of 1% Chloroprocaine in Sub-arachnoid block with or without Fentanyl for Enhanced Recovery after Perianal Surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031417
Enrollment
80
Registered
2021-02-19
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: 1% chloroprocaine: 3ml of 1% chloroprocaine for spinal anesthesia in perianal surgeries Control Intervention1: 1% chloroprocaine: For subarachnoid block, patients undergoing perianal su

Sponsors

Government medical college Patiala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of 20 -80 years of age with perianal disease

Exclusion criteria

Exclusion criteria: 1 Patientâ??s refusal 2 Any abnormality of spine 3 Any skin infection or local cellulitis. 4 Any coagulation defect. 5 Recent myocardial infarction or heart disease 6 Patients on anticoagulant drugs 7 Patients with neurological disorder

Design outcomes

Primary

MeasureTime frame
Onset of sensory and motor block Intraoperative hemodynamics Maximum sensory block Time taken to achieve maximum sensory block and for 2 segment regression of sensory blockade Time for rescue analgesia Duration of analgesia Duration of motor block Time to unassisted ambulation Time to unassisted voiding Timepoint: Sensory blockade will be assessed by loss of pinprick sensation to 23 G hypodermic needle every 2 min for 10 min until highest level is achieved then every 5 min until 2 segment regression. Motor blockade will be assessed by Modified Bromage score every 5 min till complete motor block is achieved. Intraoperative vitals will be checked every 2 min for 10 min then every 10 min till completion of surgery.

Secondary

MeasureTime frame
ComplicationsTimepoint: Intraoperatively and within 24 hours to 7 days after surgery

Countries

India

Contacts

Public ContactAmit Kaur

Government medical college, Patiala

tripat_noori@yahoo.co.in9041134956

Outcome results

None listed

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