Evaluation of the effect of topical sodium bicarbonate injection on pain after inguinal hernia surgery

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240928063193N1

Enrollment

100

Registered

2024-10-24

Start date

2024-11-20

Completion date

Unknown

Last updated

2025-01-08

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

Conditions

Unilateral indirect inguinal hernia, without obstruction or gangrene, recurrent. Unilateral inguinal hernia, without obstruction or gangrene, recurrent

Interventions

Intervention 1: In the intervention group (50 patients), a 30-minute session will be held to explain the study's objectives and the intervention process to obtain informed consent. The duration for wh

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: indirect inguinal hernia informed consent of patient not recurrence inguinal hernia

Exclusion criteria

Exclusion criteria: psychopathy Drug addiction Chronic use of Analgesics Sensory and motor disorders Complications of strangulation and gangrene loss of consciousness Patients with acute problems and needing emergency surgeries recurrent inguinal hernia

Design outcomes

Primary

Measure	Time frame
The patient's pain score is based on Visual Analogue Scale (VAS). Timepoint: 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Rahmati

Karaj University of Medical Sciences

alirahmatimd76@gmail.com+98 21 4613 0915

Outcome results

None listed

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