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Spinal versus General Anaesthesia for Ambulatory Anorectal Surgery

Comparative evaluation between Spinal Anaesthesia with Ropivacaine and General Anaesthesia for Ambulatory Anorectal surgery- A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/036048
Enrollment
80
Registered
2021-08-31
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: K928- Other specified diseases of the digestive system

Interventions

Intervention1: General anesthesia: The standard of care in ambulatory anorectal surgeries is General anesthesia. Propofol is used as the induction agent, fentanyl and morphine are given for analgesia

Sponsors

CHRISTIAN MEDICAL COLLEGEVELLORE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients suitable for ambulatory anorectal surgery (EUA and LOF+/- seton, hemorrhoidectomy, Sphincterotomy, Intersphincteric abscess drainage, etc) 2. American Society of Anaesthesiologists (ASA) physical status I and II

Exclusion criteria

Exclusion criteria: 1. Patients with chronic backache, spinal deformities, history of prolapsed intervertebral disc 2. Patients with a known history of allergy to the drugs used in the study 3. Patients with cardiac disease 4. Contraindications to spinal anaesthesia 5. Patients of ASA grade 3,4 & 5 6. Obese patient with mouth opening 7. Lack of patientâ??s consent for either technique 8. Height- extremely short or tall

Design outcomes

Primary

MeasureTime frame
To compare hemodynamic responses to surgery and anal dilatation between Spinal Anaesthesia with Ropivacaine and General AnaesthesiaTimepoint: intraoperative period, approximately one hour

Secondary

MeasureTime frame
To compare intraoperative additional anaesthetic requirementTimepoint: intraoperative period, approximately 1 hour;To compare post operative complicationsTimepoint: 4 to 6 hours;To compare post-operative pain scores Timepoint: 4 to 6 hours;To compare time to meet discharge criteriaTimepoint: 4 to 6 hours;To compare use of postoperative rescue analgesiaTimepoint: 4 to 6 hours

Countries

India

Contacts

Public ContactANJU EMMA BRILLIN

CHRISTIAN MEDICAL COLLEGE, VELLORE

anjueb1994@gmail.com6282305449

Outcome results

None listed

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