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Tamsulosin and preventing of postoperative urinary retention

Clinical trial to compare the efficacy Tamsulosin and placebo in prevention of urinary retention after general anesthesia in cataract surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012111411469N1
Enrollment
67
Registered
2013-02-11
Start date
2010-07-21
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

Cataract. Capsular glaucoma with pseudo exfoliation of lens (H40.1

Interventions

Intervention 1: Intervention 1: Tablet Tamsulosin Hydrochloride 0.4 mg, once a day for four days, Brand name Flomax , manufacturer Farabi Pharmaceutical. Intervention 2: Intervention 2: Placebo.
Prevention
Intervention 1: Tablet Tamsulosin Hydrochloride 0.4 mg, once a day for four days, Brand name Flomax , manufacturer Farabi Pharmaceutical

Sponsors

Chancellor for research, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
52 Years to 84 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : No contraindications for general anesthesia and general Surgery. Patients with spontaneous urine output less than 100 ml in the first eight hours after surgery, and completely distended palpable bladder Exclusion criteria: Congestive Heart Failure, Myocardial Infarction, Renal Failure, Hypotension (Systolic Blood Pressure less than 100 mmHg), hypersensitivity to the drug, IPSS score greater than 25 or less than 15 and patients with a permanently Foley catheter

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Urinary Retention. Timepoint: Every one hour, until 8 hours from surgery, patients will be examined for urination or probable urinary retention. Method of measurement: Failure to void and patients need to urethra catheterization.

Secondary

MeasureTime frame
Floppy Iris. Timepoint: During surgery. Method of measurement: Any iris dropping during surgery that report by surgeon and interfere with surgery.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKarampourian Arezo

Hamadan University of Medical Sciences

a.karampourian@umsha.ac ; karampor1@yahoo.com+98 81 1838 0572

Outcome results

None listed

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