Skip to content

The effect of Urtica dioica exstract on consequences of double-J ureteral catheters

The effect of Urtica dioica extract on short-time consequences of double-J ureteral catheters

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016090329680N1
Enrollment
62
Registered
2017-03-18
Start date
2017-03-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Complications of double j urethral cathater. Complications of genitourinary prosthetic devices, implants and grafts

Interventions

Intervention 1: The control group patients after discharge - the day after surgery - and for a period of 48 hours, antibiotic cefixime 400, on a daily basis and 10 ibuprofen housing 400, one pill, giv
Treatment - Drugs
The control group patients after discharge - the day after surgery - and for a period of 48 hours, antibiotic cefixime 400, on a daily basis and 10 ibuprofen housing 400, one pill, given every 8 hours
In the intervention group, in addition to these drugs, pills urtidin pharmaceutical barij company, a dosage of one pill every 8 hours, for a period of fifteen days it will be given.

Sponsors

Sharoud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the size of the stone and the location of the stone which measures (less than ten mm) and place the stone below the junction (urethral pelvic); patients suffering a urethral stone, just on one side and those who bilateral urethral stones or kidney stones are excluded; age between 20-70 years old(due to a higher incidence of kidney stones in this age range); no history of urologic manipulation in the past few years is a another criteria. Exclusion criteria: history of benign prostatic hypertrophy; previous surgery on the bladder or lower urinary tract; bladder stones; active urinary tract infection; lack of proper placement of the double J catheter; neurogenic bladder and the lack of the next visit.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Gross hematuria. Timepoint: 3 and 7 days after start of treatment. Method of measurement: questionnaire.;Dysuria. Timepoint: 3, 7 and 15 days after start of treatment. Method of measurement: questionnaire.;Frequency. Timepoint: 3, 7 and 15 days after start of treatment. Method of measurement: questionnaire.;Pain. Timepoint: 3, 7 and 15 days after start of treatment. Method of measurement: VAS score.;Microscopic hematuria. Timepoint: 15 days after start of treatment. Method of measurement: urine analysis.;Edema and inflammation of the mucus of bladder and ureter. Timepoint: 15 days after start of treatment. Method of measurement: cystoscopy.;Urinary infection. Timepoint: 15 days after start of treatment. Method of measurement: urine cuture.;Fever. Timepoint: 3, 7 and 15 days after start of treatment. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed Heydari

Clinical Research Development, Sharoud University of Medical Sciences

s.heydari91@yahoo.com+98 23 3239 5054

Outcome results

None listed

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