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The Effect of Lorazepam on Perioperative Anxiety in Patients Undergoing Elective Hernia Surgery

Comparison of the Effectiveness of Lorazepam on Perioperative Anxiety in Patients Undergoing Elective Hernia Surgery: A Double-Blind Randomized Controlled Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260226068959N2
Enrollment
68
Registered
2026-05-16
Start date
2026-04-21
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Lorazepam, Anxiety, Elective Hernia Surgery. Other long term (current) drug therapy

Interventions

Intervention 1: Intervention group: A 2mg Lorazepam tablet, is administered 6 and 18 hours before the operation. Intervention 2: Control group: A placebo tablet, identical in appearance and inactive,

Sponsors

Bojnourd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 60 Years

Inclusion criteria

Inclusion criteria: Patients scheduled for surgery under general anesthesia No history of underlying medical conditions No prior use of benzodiazepines No dependence on opioids or narcotic substances Providing informed consent to participate in the study

Exclusion criteria

Exclusion criteria: History of previous medical and psychiatric conditions emergency surgical procedures History of drug hypersensitivity Pregnancy and lactation Patients with sleep apnea Age over 60 years

Design outcomes

Primary

MeasureTime frame
Patient’s anxiety score on the State-Trait Anxiety Inventory Form Y (STAI Y). Timepoint: Morning of the surgery, After the patient regains consciousness in the recovery room, The day after the surgery. Method of measurement: State Trait Anxiety Inventory Form Y (STAI Y).

Secondary

MeasureTime frame
Patient’s pain level. Timepoint: In the recovery room and the day after surgery. Method of measurement: Visual Analogue Scale (VAS).;Patient’s sleep quality score. Timepoint: the morning of surgery, the day after surgery. Method of measurement: Leeds Sleep Evaluation Questionnaire (LSEQ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRasoul Nikdel

Bojnourd University of Medical Sciences

dr.nikdel@nkums.ac.ir+98 58 3229 6971

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026