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The effect of gabapentin supplementation in ureteral stone patients

Phase 3
Recruiting
Conditions
ureteral stone disease.
Presence of urogenital implants
Z96.0
Registration Number
IRCT20170417033489N8
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
76
Inclusion Criteria

Patients with unilateral ureteral stones more than 15 mm in diameter who have undergone TUL lithotripsy
Patients should be over 18 years old
A double G catheter is installed for them

Exclusion Criteria

Chronic use (more than 3 months) of alpha-blocker and analgesic drugs
History of neurogenic bladder
Recurrent urinary tract infections
Chronic pelvic pain
Patient dissatisfaction
Leaving the study during the study process
People who are contraindicated in gabapentin
History of previous allergy to gabapentin
Pregnancy
Breastfeeding
Liver failure
Renal failure
People who are in the high-risk group due to the drowsiness complication of the drug

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Score obtained based on the patient's irritating symptoms questionnaire. Timepoint: Before intervention and 14 days after gabapentin. Method of measurement: ureteral stent symptom questionnaire (USSQ).
Secondary Outcome Measures
NameTimeMethod
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