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Comparison of Two Methods of General Anesthesia and Spinal Anesthesia on the Time to Reach Discharge Conditions in Patients Undergoing Outpatient Perianal Surgery

Comparison of Two Methods of General Anesthesia and Spinal Anesthesia on the Time to Reach Discharge Conditions in Patients Undergoing Outpatient Perianal Surgery at Imam Khomeini Hospital Complex

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230130057273N1
Enrollment
90
Registered
2025-10-11
Start date
2025-08-23
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Hemorrhoids. Condition 2: Fissure and fistula of anal and rectal regions. Hemorrhoids and perianal venous thrombosis Fissure and fistula of anal and rectal regions

Interventions

Intervention 1: Intervention Group: Spinal Group. Spinal anesthesia will be performed under completely sterile conditions, in the sitting position, using a 25-gauge Quincke needle. The needle will be
if pain persists, 2 mg IV morphine. If morphine is given, patient stays in recovery at least one hour post-administration. Clinical status evaluated every 30 minutes via Marshall criteria. Discharge f

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 20 to 60 years ASA class I & II Type of surgery: Fissure, fistula or hemorrhoid Informed consent to participate in the plan

Exclusion criteria

Exclusion criteria: Sensitivity to anesthesia drugs used in the plan Failure of the selected method Patient position for lithotomy surgery not be Patient dissatisfaction for receiving spinal anesthesia Localized sepsis at the site of spinal Patient inability to remain immobile during spinal procedure Patient with high intra-abdominal pressure Myelopathy or peripheral neuropathy Spinal canal stenosis History of spinal column surgery in the range of spinal procedure Multiple sclerosis Spina bifida Aortic valve stenosis or fixed cardiac output Hypovolemia Thromboprophylaxis consumption in a time frame less than allowed for spinal Inherited coagulation disorder Consumption of addictive substances Surgery duration more than 90 minutes

Design outcomes

Primary

MeasureTime frame
Time to discharge readiness (based on achieving a minimum score of 9 on the Marshall criteria, assessed every 30 minutes in recovery). Timepoint: Time to discharge readiness, assessed every 30 minutes in recovery post-surgery until achieving a minimum score of 9 on the Marshall criteria. Method of measurement: Measurement method: Time to discharge readiness is assessed every 30 minutes in recovery using the Marshall criteria (Miller’s Anesthesia, 9th edition, 2020). Patients undergo standard monitoring (blood pressure, heart rate, oxygen saturation), and sensory level in the spinal group is evaluated with cold, pinprick, and touch tests. Data are analyzed using SPSS software.

Secondary

MeasureTime frame
Postoperative pain intensity. Timepoint: Immediately after surgery and every 30 minutes in recovery until discharge. Method of measurement: Numerical Rating Scale from 0 to 10.;Analgesic use in recovery. Timepoint: During patient’s stay in recovery post-surgery. Method of measurement: Recording dose and type of analgesic (ketorolac 30 milligrams intramuscularly or morphine 2 milligrams intravenously).;Postoperative shivering. Timepoint: During patient’s stay in recovery post-surgery. Method of measurement: Clinical observation and documentation of shivering by recovery staff.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Effatdoost Astane

Tehran University of Medical Sciences

reza.effatdoost@gmail.com0098 21 61190

Outcome results

None listed

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