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Compare the effect of subcutaneous injection of ketamine and lidocaine in reducing postoperative pain in patients undergoing elective inguinal hernia surgery under general anesthesia

Compare the effect of subcutaneous injection of ketamine and lidocaine in reducing postoperative pain in patients undergoing elective inguinal hernia surgery under general anesthesia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171004036561N3
Enrollment
60
Registered
2018-02-10
Start date
2017-12-22
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Inguinal Hernia. Unilateral inguinal hernia, without obstruction or gangrene

Interventions

Intervention 1: Intervention group 1: Subcutaneous injection of 1mg/kg lidocaine in the surgical cutting site. Intervention 2: Intervention group 2: Subcutaneous injection of 0/5mg/kg ketamin in the s

Sponsors

Gorgan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients undergoing elective inguinal hernia surgery under general anesthesia

Exclusion criteria

Exclusion criteria: Hypertension Hyperthyroidism History of seizure Nervous and mental illness Symptoms of increased intracranial pressure Ketamine or lidocaine allergy Liver and kidney failure Substance abuse or alcohol abuse Patient dissatisfaction Coagulation disorders Localized local infections Neurological disorders Sever Anemia

Design outcomes

Primary

MeasureTime frame
Percent reduction in pain. Timepoint: 1, 2, 4, 6 and 8 Hours after general anesthesia. Method of measurement: Visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Massoud Hosseini

Gorgan University of Medical Sciences

masoud.hoseini@webmail.goums.ac.ir+98 17 3254 2414

Outcome results

None listed

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