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Efficacy of Tamsulosin in relieving urinary symptoms due to JJ stent

Efficacy of Tamsulosin hydrochloride in relieving double j ureteral stent related morbidity-a randomized placebo controlled clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/08/004824
Enrollment
60
Registered
2014-08-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Lower urinary tract symptoms Health Condition 2: N209- Urinary calculus, unspecified

Interventions

Intervention1: Tamsulosin hydrochloride: Prescribed as Capsule 0.4 mgs at to be taken orally at bed time after meals once daily with sips of water for four weeks. Control Intervention1: Lactobacillus:

Sponsors

University College of Medical Sciences University of Delhi and GTB Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 All patients aged more than 18 to 80 years giving informed consent to participate in the study 2 Patients with urological disorders undergoing jj ureteral stenting

Exclusion criteria

Exclusion criteria: 1 Patient not willing for consent for inclusion in the above study 2 Symptomatic lower urinary tract symptoms LUTS due to BPH as diagnosed by history focused urological examination and investigations 3 Patients with pregnancy mental disorders or illness who cannot understand or comply with the study protocol 4 Patients with known history of orthostatic hypotension allergy hypersensitivity to one or more α adrenoceptor antagonists and or any component of the tamsulosin preparations 5 Patients receiving medications concomitantly in past 3 months with any alpha1 blocker

Design outcomes

Primary

MeasureTime frame
Primary outcome were assessed by USSQ VAS IPSS urinary index score pain index score general health index score work performance score and sexual matters scoreTimepoint: Third day to fourth week post intervention.

Secondary

MeasureTime frame
Secondary outcome measures were assessed by noting drug adverse events and side effects if any and overall drug tolerabilityTimepoint: Third day to fourth week post intervention

Countries

India

Contacts

Public ContactDr Sambit Tripathy

University College of Medical Sciences University of Delhi and GTB Hospital

sambit0tripathy@yahoo.co.in22586262

Outcome results

None listed

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