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Effect of spinal anesthesia on postoperative pain

Comparing postoperative pain in Laparoscopic cholecystectomy under spinal anesthesia with general anesthesia in symptomatic cholelithiasis: A randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200718048125N1
Enrollment
32
Registered
2020-12-26
Start date
2018-06-13
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

cholelithiasis. Cholelithiasis

Interventions

Intervention 1: Intervention group: Spinal anesthesia
26-gauge spinal needle (Dr.J Tianjin Hanaco Medical Co. Tianjin, China) was introduced, then 0.5% Bupivacaine mixed with 0.2 µg of Sufentanil was injected at either the third or fourth lumbar epidural
5 mg/kg Thiopentone Sodium, 0/5 mg/kg Atracurium Besylate, 2 mg Midazolam, 3 µg/kg Sufentanil were administered, then 100 µg/kg/min Propofol mixed with N2O were infused.

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients diagnosed with symptomatic cholelithiasis Patients with body mass index of less to equal of 32 Kg/m2 Patients with American Society of Anesthesiologists (ASA) physical status I, II, and III.

Exclusion criteria

Exclusion criteria: having a history of severe nausea and vomiting in last 24 hours using antiemetics in the last 24 hours using analgesic medications in the last 48 hours having an allergic response to anesthetics having coagulopathy disorders seen deformity of vertebral bones addiction or drug abuse having skin injury in the place of injection for anesthesia

Design outcomes

Primary

MeasureTime frame
Postoperative pain. Timepoint: during recovery and 2, 4 hours after surgery. Method of measurement: Visual Analogue Scale.;Heart rate. Timepoint: before surgery, after induction, first, second, third 15 minutes after surgery and in recovery. Method of measurement: Clinical examination.;Mean arterial pressure. Timepoint: First, second, and third 15 minutes after surgery. Method of measurement: Clinical examination.;Postoperative nausea and vomiting. Timepoint: during recovery. Method of measurement: Clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamed Beyzaii

Islamic Azad University

hmd_beyzaii@yahoo.com+98 51 3225 6291

Outcome results

None listed

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