Skip to content

The effect of group patient education before PCNL surgery on SIRS index

Investigating the effect of group training of pre-operative tubeless PCNL patients on postoperative SIRS index

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200905048625N4
Enrollment
100
Registered
2025-06-14
Start date
2025-08-11
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Kidney stones. Acute tubulo-interstitial nephritis

Interventions

Intervention 1: Control group: Patients in the control group do not receive any group education and only experience routine preoperative care. Intervention 2: Intervention group: Patients receive a gr

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients over 18 years of age are candidates for PCNL surgery. Patients with no history of mental illness or chronic pain. Written and informed consent from patients

Exclusion criteria

Exclusion criteria: Patients with a history of mental illness and use of psychiatric medications Patients taking strong painkillers or anti-inflammatory drugs regularly. Patients with a history of addiction and use of narcotics and opioids Patients with a history of chronic inflammatory disease Patients with severe immunodeficiency (such as HIV positive or undergoing intensive corticosteroid treatments). Any patient with contraindications for PCNL. Patients with any of the following conditions that may interfere with SIRS: History of corticosteroid or chemotherapy treatment. Fever and active infection. CRP greater than 50 mg/L. Diabetes. Systemic inflammatory diseases. Positive urine culture. Rhinal anomalies (such as horseshoe kidney). History of urinary stone surgery. Use of Double J.

Design outcomes

Primary

MeasureTime frame
The impact of group patient education on clinical outcomes. Timepoint: 24 hours, 48 ??hours and 7 days after surgery. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Akram Mirzaei

Tehran University of Medical Sciences

mirzaee.scholar@gmail.com+98 21 6634 8560

Outcome results

None listed

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