Clinical Trials Directory

Trials / Completed

CompletedNCT02008864

Evaluating the Effect of Senna in Uremic Pruritus

Phase II Study of the Effect of Senna Alexandrina Mill. on Uremic Pruritus and Serum IL-2, INF-δ and TNF-α Levels of Hemodialysed Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Shiraz University of Medical Sciences · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Uremic pruritus remains one of the most frustrating and potentially disabling symptoms in patients with end stage renal disease. It affect up to 90 percent of patients with end stage renal disease. Several hypotheses have been postulated for the possible underlying etiology, but none is conclusive. Aside from kidney transplantation, which is only definitive treatment, therapeutic approaches have largely been empirical, and no firm evident-base treatments are available. The main goal of therapy remains to minimize severity of pruritus. In Iranian traditional medicine Cassia senna L. is used for healing uremic pruritus . In this study investigators considered to evaluate effect of Cassia senna L. in uremic pruritus by a double blind placebo control clinical trial. It is hypothesized that oral Cassia senna L. may attenuate uremic pruritus by decreasing serum IL-2, IFN-γ and TNF-α.

Conditions

Interventions

TypeNameDescription
DRUGSenna(7.5 mg of sennosoides A and B) Senna tablet/ 2 times per day
DRUGPlaceboPlacebo tablet/ 2 times per day

Timeline

Start date
2011-08-01
Primary completion
2012-09-01
First posted
2013-12-11
Last updated
2015-04-01

Source: ClinicalTrials.gov record NCT02008864. Inclusion in this directory is not an endorsement.