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Clinical Trials/CTRI/2014/09/005000
CTRI/2014/09/005000
Recruiting
Phase 4

A prospective, comparative study of the incidence and severity of constipation with darifenacin and trospium in overactive bladder.

Self Dr Manjunatha R0 sites30 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Self Dr Manjunatha R
Enrollment
30
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Self Dr Manjunatha R

Eligibility Criteria

Inclusion Criteria

  • Male and female patients aged \>\=18 and \<80 years who were diagnosed with OAB based on their overactive bladder symptoms.
  • Patients with a baseline score for urinary urgency of \>\=2 points, day time frequency \>1 point and a total OABSS of \>\=3 points, with or without urgency urinary incontinence (UUI) episodes
  • Patients with stable doses of alpha blockers or 5\-alpha\-reductase inhibitors for patients with benign prostatic hyperplasia were permitted with the limitation that a specific drug was used without a change in dosage and administration and was not replaced with another drug during the study period (observation and treatment phase).

Exclusion Criteria

  • Serious heart disease,
  • Untreated angle\-closure glaucoma,
  • Myasthenia gravis,
  • Gastric outlet and intestinal obstruction, paralytic ileus, gastric and intestinal atony or risk of urinary or gastric retention.
  • Residual urine volume \>\=100 mL (determined by abdominal sonography)
  • Strong possibility of prostate and bladder cancer
  • Acute active urinary tract infection
  • Women of childbearing age were required not to be pregnant or nursing, and to be using acceptable methods of contraception.
  • Concomitant treatments known to affect urinary bladder function like anticholinergics, antispasmodics, serotonin\-noradrenaline\-reuptake\-inhibitors, TCA, first generation antihistaminics, cholinergic agonists, cholinesterase inhibitors (e.g. bethanecol, donepezil and rivastigmine), potent inhibitors of cytochrome CYP3A4 (e.g. ketoconazole, itraconazole, ritonavir, nelfinavir, clarithromycin and nefazadone), potent P\-glycoprotein inhibitors (e.g. cyclosporine and verapamil), aluminum antacids, antiparkinson and antipsychotic drugs, Calcium channel blockers, opioids, muscle relaxants, angiotensin\-converting enzyme inhibitors, anticoagulants.
  • Severe hepatic or renal dysfunction

Outcomes

Primary Outcomes

Not specified

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