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CHLOROPROCAINE WITH OR WITHOUT FENTANYL FOR SPINAL ANAESTHESIA

Comparison of Chloroprocaine with or without fentanyl for perianal day care procedures under subarachnoid block: a randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/010811
Enrollment
40
Registered
2017-12-07
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: K61- Abscess of anal and rectal regions Health Condition 2: K60- Fissure and fistula of anal and rectal regions Health Condition 3: null- Perianal procedures

Interventions

Intervention1: Subarachnoid block: Subarachnoid block will be administered and one of the group patients will receive Chloroprocaine with normal saline (control group) and the other group will receive

Sponsors

University College of Medical Sciences and Guru Teg Bahadur Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: A total of 40 patients (20 in each group) of either sex between 18-60 years of age belonging to ASA physical status I and II, about to undergo elective perianal surgeries under SAB of expected duration between 30-60 minutes will be recruited

Exclusion criteria

Exclusion criteria: 1. Non-consenting for SAB. 2. Patient with contraindication to SAB like coagulation disorders, local site infection, raised intracranial tension, on anti-platelet therapy etc. 3. Patient with known hypersensitivity to any of the drugs used in the study. 4. Patient with height 180 cm.

Design outcomes

Primary

MeasureTime frame
Sensory block durationTimepoint: Once, at the time of request of first rescue analgesia

Secondary

MeasureTime frame
Sensory block onset Maximum height of sensory block achieved Time taken to achieve maximum height of sensory block Time to two dermatomal regression Intensity and quality of motor block Hemodynamic profiles Time to home readinessTimepoint: Every 5 min intra-operative and every 15 min post-operative till 90 min

Countries

India

Contacts

Public ContactDr Srivignesh P

University College of Medical Sciences

rsramb@gmail.com9868399699

Outcome results

None listed

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